WO2022223033A1 - Sos1 degrading agent and preparation method therefor and application thereof - Google Patents

Sos1 degrading agent and preparation method therefor and application thereof Download PDF

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WO2022223033A1
WO2022223033A1 PCT/CN2022/088560 CN2022088560W WO2022223033A1 WO 2022223033 A1 WO2022223033 A1 WO 2022223033A1 CN 2022088560 W CN2022088560 W CN 2022088560W WO 2022223033 A1 WO2022223033 A1 WO 2022223033A1
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alkyl
membered
cycloalkyl
heterocycloalkyl
hydrogen
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PCT/CN2022/088560
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French (fr)
Chinese (zh)
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叶正清
冯焱
李世强
丁陈利
王俏
韦红
谢舒晨
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上海领泰生物医药科技有限公司
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Priority to JP2023560092A priority Critical patent/JP2024516518A/en
Priority to US18/556,862 priority patent/US20240261417A1/en
Priority to EP22791138.5A priority patent/EP4328219A1/en
Publication of WO2022223033A1 publication Critical patent/WO2022223033A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/545—Heterocyclic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-condensed systems

Definitions

  • the present invention belongs to the technical field of medicine, and specifically, the present invention relates to a SOS1 degrading agent, a preparation method thereof, and its application as a therapeutic agent for preventing and/or treating cancer.
  • SOS1 (son of sevenless homolog 1) protein is a regulatory protein that is widely expressed in cells. As a key protein in signaling pathways, SOS1 plays an important regulatory role in many signal transduction pathways in cells, such as the regulation of Ras and Rac signaling pathway.
  • SOS1 consists of 1333 amino acids and contains a proline-rich domain (PxxP) at its C-terminus, which can interact with growth factor receptor-bound protein 2 (growth factor receptor-bound protein 2) in the Ras pathway.
  • Grb2 combined to form a complex of Grb2 and SOS1, thereby bringing SOS1 to the vicinity of Ras protein in the cell membrane.
  • SOS1 catalyzes the combination of Ras and GTP, promotes the activation of Ras, and then activates multiple downstream signaling pathways, such as Ras-Raf-Mek -Erk, Ras-PI3K-AKT-mTOR.
  • PxxP can also bind to the SH3 (Src homology 3) domain of proteins such as E3B1 in the Rac pathway to form EPS8-E3B1-SOS1 complexes, which connect actin filaments through EPS8, causing GTP switch, thereby activating Rac, which subsequently activates signaling pathways such as JNK and MAPK.
  • Ras mutation gene is considered to be the main oncogene with high incidence of human cancer. Studies have shown that Ras mutation exists in 20-30% of tumor patients, among which KRas mutation accounts for 85%, NRas and HRas account for 12% respectively and 3%. However, directly acting on Ras to inhibit its activity is considered extremely challenging due to the picomolar affinity of GTP for its binding site and the smooth surface of Ras protein and lack of other suitable binding pockets.
  • SOS1 The abnormal expression or mutation of SOS1 is also closely related to the occurrence of clinical diseases. Studies have shown that SOS1 mutations exist in NS patients and CFC patients. HGF1 is a rare autosomal dominant genetic disease, and its etiology is also related to the mutation of the PxxP domain of SOS1. In addition, abnormal expression or mutation of SOS1 is associated with The occurrence of cancer is also related.
  • WO2018172250A1 discloses several types of SOS1 inhibitors, but so far, there is no relevant report on SOS1 degraders.
  • Protein degradation targeting chimera is a technology different from traditional small molecule inhibitors, traditional small molecule inhibitors usually need to act on the active site of the target protein to inhibit its activity, while PROTAC is a A heterogeneous bifunctional molecule, one end of which is a small molecule inhibitor that can recognize the target protein, and the other end is an E3 ubiquitin ligase ligand that can recognize E3 ubiquitin ligase.
  • This bifunctional molecule is in vivo It recognizes the target protein and E3 ubiquitin ligase, and draws the target protein and E3 ubiquitin ligase closer to form a ternary complex.
  • the target protein After ubiquitinating the target protein, the target protein is degraded in vivo through the ubiquitin-proteasome pathway. Compared with traditional small molecule inhibitors, PROTAC only needs to bring the target protein closer to E3 ubiquitin ligase to degrade the substrate.
  • the present invention provides compounds of formula I, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable compounds thereof the salt
  • S is a small molecule compound that can inhibit the activity of SOS1 protein or bind to SOS1 protein;
  • L is the linking chain, which connects S and E by covalent bonds
  • E is the small molecule ligand of the E3 ubiquitin ligase complex.
  • the present invention provides compounds of formula I, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable compounds thereof the salt
  • the S is S1:
  • R 1 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8
  • R 1 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 6-10 membered aryl or 5-10 membered heteroaryl;
  • R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 1 is -NH-(CH 2 ) k -NH-C(O)-R aa , wherein R aa is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl (eg, said R aa is C 1 -C 6 alkyl), and k is 1 or 2;
  • R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
  • C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR
  • R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
  • a 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl (eg phenyl) or heteroaryl (eg thienyl);
  • R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6
  • R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl or -C(O)C 1 -C 3 alkyl;
  • R 2 is -C(O)NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
  • R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
  • R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
  • R 2 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkane base;
  • w is 1, 2, 3, or 4 (eg, the w is 1, 2, or 3);
  • the A 2 (R 3 ) Y is hydrogen
  • a 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl (eg phenyl) or heteroaryl, and
  • R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 7 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
  • alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
  • alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl
  • the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1
  • the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt
  • the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 al
  • R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 N(CH 3 ) 2 ;
  • R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)O R z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
  • R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
  • R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
  • Y is 0, 1, 2, 3, 4, or 5 (eg, Y is 0, 1, 2, or 3);
  • R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace.
  • each of R 4 and R 5 in the S1 is independently a methyl group.
  • the R a and R b at any one occurrence are each independently hydrogen or C 1 -C 6 alkyl.
  • the Rd and Re at any one occurrence are each independently hydrogen or C1 - C6 alkyl.
  • R 5 is a C 1 -C 6 alkyl group, such as methyl.
  • R 4 is a C 1 -C 6 alkyl group, such as methyl.
  • R 1 is hydrogen or C 1 -C 6 alkoxy.
  • a 1 is an aryl group or a heteroaryl group.
  • a 1 is an aryl group, such as a phenyl group.
  • a 1 is a heteroaryl group, such as a thienyl group.
  • R 2 is hydrogen, halogen, C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 2 is an aryl group, such as a phenyl group.
  • R 3 is hydrogen, halogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted by -NR k R l ; the R k and R l are each independently hydrogen or C1 - C6 alkyl.
  • R 3 is hydrogen, F, Cl, methyl or ethyl, and the methyl and ethyl are substituted by -NR k R 1 ; the R k is methyl or ethyl, R l is hydrogen, methyl or ethyl.
  • R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
  • a 1 is an aryl group
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 1 is a heteroaryl group
  • L' is a bond
  • a 2 is an aryl group
  • R 3 is hydrogen, halogen or C 1 -C 6 alkyl group, the alkyl group optionally substituted with -NRkRl ; said Rk and Rl are each independently hydrogen or C1 - C6 alkyl.
  • the S is S1':
  • the S is S1":
  • R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
  • R 1 is hydrogen, methyl, methoxy or
  • Fragment is
  • the S is -X-S1', and the structure of S1' is as described above;
  • X is O, NH or S, preferably O.
  • the S is -X-S1", and the structure of S1" is as described above;
  • X is O, NH or S, preferably O.
  • the S is S1a
  • x is 1 or 2;
  • a 1 is selected from
  • w 1, 2 or 3;
  • Y is 1 or 2;
  • w is 1 or 2.
  • R 1 is hydrogen, -CH 3 , -OCH 3 , -OCH 2 CH 3 , -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 or -O( CH2 ) 3CH3 , eg -OCH3 .
  • a 1 is
  • a 1 is
  • R 2 is hydrogen, halogen, -NH 2 , C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 2 is
  • R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH2 -N( CH3 ) 2 or -CH2 -NH - CH2CH3 .
  • R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
  • a 1 is L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 1 is L' is the key
  • a 2 is R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 or -CH 2 -NH - CH2CH3 .
  • the S is S1a':
  • R 1 , R 2 , R 3 , L', A 1 , A 2 , w, x and Y are as described in S1 or S1a.
  • the S is S1a":
  • R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
  • R 1 is hydrogen, methyl, methoxy or
  • the S is -X-S1a', and the structure of S1a' is as described above;
  • X is O, NH or S, preferably O.
  • the S is -X-S1a", and the structure of S1a" is as described above;
  • X is O, NH or S, preferably O.
  • the S1 is the specific compound of Example 1 (Example 1) to Example 458 (Example 458) in WO2018172250A1 (which is incorporated herein by reference in its entirety).
  • the S is S2:
  • R 1 is hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkyl mercapto or -NR a R b ; the R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8
  • R 1 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl;
  • R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, C 1 -C 6 alkyl , C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 1 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
  • R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
  • C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR
  • R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
  • L 2 a is C(O)
  • L 2 b is bond or C 1 -C 6 alkylene
  • X 2 is
  • said x is 1, 2, 3, or 4 (eg, said x is 1, 2, or 3);
  • a 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl;
  • R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6
  • R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 2 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
  • R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
  • R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
  • R 2 is -(CH 2 )NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl, or C 3 -C 8 ring alkyl;
  • w is 1, 2, 3, or 4 (eg, the w is 1 or 2);
  • the A 2 (R 3 ) Y is hydrogen
  • a 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl, and
  • R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 2 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
  • alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
  • alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl
  • the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1
  • the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt
  • the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 al
  • R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 NH(CH 3 ) 2 ;
  • R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)O R z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
  • R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
  • R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
  • Y is 0, 1, 2, 3, 4, or 5 (eg, the Y is 0, 1, 2, or 3);
  • R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace;
  • Both T and V are N, or T is C and V is N, or T is N and V is C.
  • each of R 4 and R 5 in the S2 is independently a methyl group.
  • each of said Ra and Rb at any occurrence is independently hydrogen or C1 - C6 alkyl.
  • both T and V are N.
  • T is C
  • V is N
  • T is N
  • V is C
  • R 5 is a C 1 -C 6 alkyl group, such as methyl.
  • R 4 is a C 1 -C 6 alkyl group, such as methyl.
  • R 1 is hydrogen or C 1 -C 6 alkoxy.
  • a 1 is an aryl group or a heteroaryl group.
  • a 1 is an aryl group, such as a phenyl group.
  • a 1 is a heteroaryl group, such as a thienyl group.
  • R 2 is hydrogen, halogen, C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 2 is an aryl group, such as a phenyl group.
  • R 3 is hydrogen, halogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted by -NR k R l ; the R k and R l are each independently hydrogen or C1 - C6 alkyl.
  • R 3 is hydrogen, F, Cl, methyl or ethyl, and the methyl and ethyl are substituted by -NR k R 1 ; the R k is methyl or ethyl, R l is hydrogen, methyl or ethyl.
  • R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
  • a 1 is an aryl group
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 1 is a heteroaryl group
  • L' is a bond
  • a 2 is an aryl group
  • R 3 is hydrogen, halogen or C 1 -C 6 alkyl group, the alkyl group optionally substituted with -NRkRl ; said Rk and Rl are each independently hydrogen or C1 - C6 alkyl.
  • the S is S2':
  • the S is S2":
  • R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C 6 alkoxy optionally substituted with C 1 -C 6 alkoxy (eg, methoxy).
  • R 1 is hydrogen, methyl, methoxy or
  • Fragment is
  • the S is -X-S2', and the structure of S2' is as described above;
  • X is O, NH or S, preferably O.
  • the S is -X-S2", and the structure of S2" is as described above;
  • X is O, NH or S, preferably O.
  • the S is S2a
  • Both T and V are N, or T is C and V is N, or T is N and V is C;
  • z is 1 or 2;
  • x is 1 or 2;
  • a 1 is selected from
  • w 1, 2 or 3;
  • Y is 1 or 2;
  • the S2 is the specific compound of Example 1 (Example 1) to Example 100 (Example 100) in WO2019201848A1 (the entirety of which is incorporated herein by reference).
  • w is 1 or 2.
  • R 1 is hydrogen, methyl, -OCH 3 , -OCH 2 CH 3 , -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 or -O(CH 2 ) 3 CH 3 , eg -OCH 3 .
  • a 1 is
  • a 1 is
  • R 2 is hydrogen, halogen, -NH 2 , C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
  • L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 2 is
  • R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH2 -N( CH3 ) 2 or -CH2 -NH - CH2CH3 .
  • R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
  • a 1 is L' is a bond
  • a 2 (R 3 ) Y is hydrogen
  • a 1 is L' is the key
  • a 2 is R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 or -CH 2 -NH - CH2CH3 .
  • the S is S2a'
  • the S is S2a
  • T, V, R 2 , R 3 , L', A 1 , A 2 , w and Y are as described in S2 or S2a.
  • R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
  • R 1 is hydrogen, methyl, methoxy or
  • the S is -X-S2a', and the structure of S2a' is as described above;
  • X is O, NH or S, preferably O.
  • the S is -X-S2a", and the structure of S2a" is as described above;
  • X is O, NH or S, preferably O.
  • the S is S3:
  • Q 1 and Q 2 are each independent CH or N;
  • Q 3 , Q 4 and Q 7 are independently C or N, at least one of said Q 3 and Q 4 is C, and not all of said Q 3 , Q 4 and Q 7 are N;
  • Q 5 is CH, N, NH, O or S
  • Q 6 is CH, N, NH, N(C 1 -C 6 alkyl), N(C 1 -C 6 heteroalkyl), N(3-7 membered cycloalkyl), N(3-7 membered heteroalkyl) ring), O or S;
  • At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 , Q 6 and Q 7 is N, NH, O or S;
  • R 1 is selected from hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, halogen, -NHR 1a , -OR 1a , C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or -CN; the C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl and C 3 -C 6 cycloalkoxy are optionally selected from halogen, Substituent substitution of -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
  • R 2 is selected from hydrogen, halogen, -CN, -NO 2 , C 1 -C 6 alkylmercapto, C 2 -C 6 alkynyl, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, -NR 2b R 2c , -OR 2a , 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-10-membered heteroaryl; the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5-
  • the 10-membered heteroaryl groups are each independently optionally selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl,
  • the R 2b is hydrogen or C 1 -C 6 alkyl
  • the R 2c is hydrogen or C 1 -C 6 alkyl
  • R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, C 1 -C 6 alkyl , C 3 -C 8 heterocycloalkyl, or C 3 -C 8 cycloalkyl (eg, the R a and R b are each independently hydrogen or C 1 -C 6 alkyl);
  • R 2 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
  • R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
  • R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or C 3 -C 6 cycloalkoxy; at least one of said R 3 and R 4 is not hydrogen, or the R 3 and R 4 and the atoms to which they are attached together form a 3-6 membered cycloalkyl; the alkyl, alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or halogen substituted;
  • A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 Substituted, R2 is as defined in S1 ) 5-6 membered heteroaryl.
  • the S is S3a
  • Q 1 and Q 2 are each independent CH or N;
  • Q 3 and Q 4 are independently C or N, and at least one of the Q 3 and Q 4 is C;
  • Q 6 is CH, N, NH, O or S
  • Q 5 is CH, N, NH, O or S
  • At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 and Q 6 is N, NH, O or S;
  • R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -OR 1a , cyclopropyl or -CN; said R 1a is hydrogen or C 1 -C 6 alkyl;
  • L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
  • R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; said q is an integer from 1 to 5; said 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5 -10-membered heteroaryl groups are each independently optionally substituted with a substituent selected from C 1 -C 6 alkyl, -OH, halogen, -C(O)R 2a , -C(O)NR 2b R 2c ;
  • the R 2a is C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 , the r is 1, 2 or 3; the R 2b is hydrogen or
  • R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is not hydrogen, or said R 3 and R 4 together with the atoms to which they are attached form 3 -6-membered cycloalkyl;
  • A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) phenyl or optionally substituted (eg optionally substituted with 1 or more R2, R2 2 is as defined in S1) 5-6 membered heteroaryl.
  • the S3 is a specific compound of Example 1 (Example 1) to Example 103 (Example 103) in WO2020180768A1 (the entirety of which is incorporated herein by reference).
  • the S is S4:
  • Q 1 is CH or N
  • Q 4 is CH, C or N
  • Each Q 2 is independently CR 1 or N, and one of the Q 2 is N and the other Q 2 is CR 1 ;
  • Each Q 3 and Q 5 molecule is independently C(R QC ) 2 , NR QN , C(O), O, S, or SO 2 , and each R QC is independently hydrogen, F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
  • At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
  • n 0, 1, 2 or 3;
  • n 0, 1, 2 or 3;
  • R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -C(O)NHR 1a , -NHR 1a , -OR 1a , cyclopropyl, azetidine or -CN; the C 1 - C6 alkyl and azetidine are optionally substituted with substituents selected from halogen, R 1a , -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, cyclopropyl base, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
  • the R 2b is hydrogen or C 1 -C 6 alkyl
  • the R 2c is hydrogen or C 1 -C 6 alkyl
  • R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl optionally substituted by halogen, -OH, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and The atoms to which it is attached together form a 3-6 membered cycloalkyl;
  • A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 substituted, R is as defined in S1 ) 5-6 membered heteroaryl;
  • condition is when for or , R 1 is not hydrogen.
  • the S is S4a
  • Q 1 is CH or N
  • Q 4 is CH, C or N
  • Each Q 2 is independently CR 1 or N;
  • Each Q3 and Q5 molecule is independently C( RQC ) 2 , NRQN , C(O), O, S, or SO2, and each RQC is independently hydrogen , F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
  • At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
  • R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, cyclopropyl, cyano or -OR 1a , said R 1a is hydrogen or C 1 -C 6 alkyl;
  • L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
  • R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; the q is a multiple of 1 to 5; the 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-membered -10-membered heteroaryl groups are each independently optionally substituted with a group selected from C 1 -C 6 alkyl, hydroxy, halogen, -C(O)R 2a or -C(O)NR 2b R 2c ; the The R 2a is selected from C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 ; the r is 1, 2 or 3; the
  • R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and the atoms to which they are attached together form a 3- 6-membered cycloalkyl;
  • A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 Substituted, R2 is as defined in S1 ) 5-6 membered heteroaryl.
  • R 3 and R 4 in the S4a are each independently hydrogen or methyl, and at least one of the R 3 and R 4 is hydrogen.
  • the S4 is the specific compound of Example 1 (Example 1) to Example 540 (Example 540) in WO2020180770A1 (which is incorporated herein by reference in its entirety).
  • the S is S5:
  • the R 1 is hydrogen or R a1 ;
  • R a1 is selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 Cycloalkenyl, 3-10-membered heterocycloalkyl, C 6 -C 10 -membered aryl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 membered aryl and 5-10 membered heteroaryl is optionally substituted with one or more identical or different R b1 and/or R c1 ;
  • Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4alkyl )C(O)R c1 , -NHC(O) OR c1 or -N(C 1 -C 4 alkyl)C(O)OR c1 ;
  • Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl; the C 1 -C 6 alkyl, C 1 -C 6 Haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C
  • the 10 -aryl and 5-10-membered heteroaryl groups are each independently optionally surrounded by 1 or more identical or different R d1 and/or R e1 ;
  • Each R d1 is independently -OR e1 , -NR e1 R e1 , halogen, -CN, -C(O)R e1 , -C(O)OR e1 , -C(O)NR e1 R e1 , - S(O) 2 R e1 , -S(O) 2 NR e1 R e1 , -NHC(O)R e1 , -N(C 1 -C 4 alkyl)C(O)R e1 , -NHC(O) OR e1 or -N(C 1 -C 4 alkyl)C(O)OR e1 ;
  • Each R e1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl;
  • R 2 is selected from hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl or halogen;
  • Ring A is selected from C 6 -C 10 aryl, 5-10 membered heteroaryl or 9-10 membered biheterocycloalkyl;
  • p 1, 2 or 3;
  • Each R 4 is independently hydrogen, hydroxy, oxo, halogen, cyano, C 1 -C 4 alkyl, -NH 2 , C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy, 3-6 membered heterocycle Alkyl, C 3 -C 6 hydroxycycloalkyl, C 1 -C 4 haloalkyl substituted by 3-6 membered heterocycloalkyl, substituted by hydroxy, halogen, -NH 2 , -S(O) 2 -(C 1 -C 4 alkyl) or oxo-substituted 3-6 membered heterocycloalkyl, and the oxo group is only substituted on a
  • R 4 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 4 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
  • R 4 is -C(O)OR g , and said R g is hydrogen or C 1 -C 6 alkyl;
  • R 4 is -OR h ; Described R h is C 1 -C 6 alkyl;
  • R 4 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
  • R 3 and R 5 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkane radical, alkoxy, cycloalkyl and cycloalkoxy optionally by cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen substituted.
  • R 5 in the S5 is methyl.
  • the Ra and Rb at any one occurrence are each independently hydrogen or C1 - C6 alkyl.
  • the S is S5':
  • the S is -X-S5', and the structure of S5' is as described above;
  • X is O, NH or S, preferably O.
  • the S is S5a:
  • R 1 , R 2 , R 3 , R 4 , ring A and p are as defined and described in S5.
  • the S is S5a':
  • the S is -X-S5a', and the structure of S5a' is as described above;
  • X is O, NH or S, preferably O.
  • the S5 is a specific compound of I-1 to I-179 in WO2019122129A1 (which is incorporated herein by reference in its entirety).
  • the S is S6:
  • R 2 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 2 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy (eg ), C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl (eg ), 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloC alkane 3 -yl C 8 , cyclophenylalkyl, or hetero-aryl C 4 -yl C, 8 C ring 1 -alkenyl C 6 group; haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C
  • R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , and said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
  • R 2 is -NH-(CH 2 ) k -NH-C(O)-R aa which is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl, and k is 1 or 2;
  • R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
  • C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR
  • R 2 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
  • R 1 is hydrogen or -OR A ;
  • R A is hydrogen, C 3 -C 10 cycloalkyl or 3-10 membered heterocycloalkyl; the C 3 -C 10 cycloalkyl and 3-10 membered heterocycloalkyl are optionally composed of one or more same or different R a1 and/or R c1 substitutions;
  • Each R a1 is independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3 -10-membered heterocycloalkyl or 5-10-membered heteroaryl; said C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are each independently optionally substituted by one or more identical or different R b1 and/or R c1 ;
  • Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4 alkyl)C(O)R c1 , oxo substituted , and the oxo group is only substituted on a non-aromatic ring;
  • Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl , 3-10 membered heterocycloalkyl or 5-10 heteroaryl;
  • R 1 is selected from C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl; the C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl are optionally surrounded by one or more R a2 and/or R b2 substitutions;
  • Each R a2 is independently selected from C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkane base, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl optionally substituted by 1 or more R c2 and/or R b2 ;
  • Each R c2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d2 and/or R e2 ;
  • Each R d2 is independently -OR e2 , -NR e2 Re2 , halogen, -CN, -C(O)R e2 , -C(O)OR e2 , -C(O)NR e2 Re2 , - S(O) 2 R e2 , -S(O) 2 NR e2 R e2 , -NHC(O)R e2 , -N(C 1 -C 4 alkyl)C(O)R e2 , oxo, all The oxo group is only substituted on a non-aromatic ring;
  • Each R e2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R f2 and/or R g2 ;
  • Each R f2 is independently selected from -OR g2 , -NR g2 R g2 , halogen, -CN, -C(O)R g2 , -C(O)OR g2 , -C(O)NR g2 R g2 , -S(O) 2 R g2 , -S(O) 2 NR g2 R g2 , -NHC(O)R g2 , -N(C 1 -C 4 alkyl)C(O)R g2 , oxo,
  • the oxo group is only substituted on a non-aromatic ring;
  • Each R g2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
  • R 1 is selected from C 2 -C 4 alkyl, C 2 -C 4 alkenyl; the C 2 -C 4 alkyl and C 2 -C 4 alkenyl are optionally substituted by R b3 ;
  • R b3 is selected from -C(O)R c3 , -C(O)OR c3 , -C(O)NR c3 R c3 , -C(O)NHOR c3 or -C(O)N(C 1 -C 4 alkyl) OR c3 ;
  • Each R c3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d3 and/or R e3 ;
  • Each R d3 is independently selected from -OR e3 , -NR e3 R e3 , halogen, -CN, -C(O)R e3 , -C(O)OR e3 , -C(O)NR e3 R e3 , -S(O) 2 R e3 , -S(O) 2 NR e3 R e3 , -NHC(O)R e3 , -N(C 1 -C 4 alkyl)C(O)R e3 , oxo,
  • the oxo group is only substituted on a non-aromatic ring;
  • Each R e3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
  • R 3 is selected from hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl), -N(C 1 -C 4 alkyl) 2 or halogen;
  • R 5 is selected from hydrogen, hydroxyl or -NHR';
  • R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
  • R 4 is selected from C 1 -C 4 alkyl, hydroxy, oxo, cyano, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 2 -C 6 alkenyl, -C 2 -C 6 alkynyl, C 3 -C 6 cycloalkoxy, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl , 3-6 membered hydroxy heterocycloalkyl, halogen or -SO 2 -C 1 -C 4 alkyl;
  • R 6 is selected from hydrogen, C 1 -C 4 alkyl or halogen
  • R 7 and R 8 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace.
  • the Fragment is E.g
  • R 1 is hydrogen or -OR A
  • RA is hydrogen
  • R 1 is hydrogen
  • R 2 is hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl) ), -N(C 1 -C 4 alkyl) 2 or halogen, said C 1 -C 4 alkyl and -O(C 1 -C 4 alkyl) are each independently optionally -O(C 1 - C 4 alkyl) substituted.
  • R 2 is hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl) ), -N(C 1 -C 4 alkyl) 2 or halogen.
  • R 2 is hydrogen, C 1 -C 4 alkyl or -O(C 1 -C 4 alkyl), and -O(C 1 -C 4 alkyl) is any Optionally substituted with -O(C 1 -C 4 alkyl).
  • R 2 is
  • R3 is hydrogen
  • R 5 is hydrogen or -NHR'.
  • R 4 is C 1 -C 4 haloalkyl
  • R 6 is hydrogen or halogen
  • R 4 , R 6 and the carbon atom to which they are attached together form a ring such that the Fragment is
  • R 7 is C 1 -C 6 alkyl.
  • R 8 is C 1 -C 6 alkyl.
  • R 1 is hydrogen or -OR A ;
  • R A is hydrogen
  • R 2 is hydrogen, C 1 -C 4 alkyl, or -O(C 1 -C 4 alkyl) (eg, methoxy), optionally -O(C 1 -C 4 alkyl) (C 1 -C 4 alkyl) (eg methoxy) substituted;
  • R 3 is hydrogen
  • R 5 is hydrogen or -NHR'
  • R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
  • R 4 is C 1 -C 4 haloalkyl
  • R 6 is hydrogen or halogen
  • R 4 , R 6 and the carbon atoms to which they are attached together form a ring so that the Fragment is
  • R 7 is C 1 -C 6 alkyl
  • R 8 is C 1 -C 6 alkyl.
  • the C 1 -C 4 alkyl may be methyl.
  • the -O(C 1 -C 4 alkyl) may be -OCH 3 .
  • R 2 is hydrogen, methyl, -OCH 3 or
  • R 2 is hydrogen, methyl or -OCH 3 .
  • R3 is hydrogen
  • the C 1 -C 3 alkyl group may be ethyl or isopropyl.
  • the -C(O)C 1 -C 3 alkyl can be -C(O ) CH 3 .
  • R 5 is hydrogen or -NHR', wherein R' is hydrogen, ethyl, isopropyl or -C(O)CH 3 .
  • R 5 is -NHR', wherein R' is hydrogen.
  • R 4 is C 1 -C 4 haloalkyl
  • R 6 is hydrogen or halogen
  • R 4 , R 6 and the carbon atoms to which they are attached together form a ring so that the Fragment is
  • the C 1 -C 4 haloalkyl may be C 1 -C 4 fluoroalkyl, such as trifluoromethyl base.
  • R 7 is C 1 -C 6 alkyl.
  • the C 1 -C 6 alkyl group may be a methyl group.
  • R 8 is C 1 -C 6 alkyl.
  • the C 1 -C 6 alkyl group may be a methyl group.
  • the S6 Fragments can be any type of S6 Fragments.
  • the S6 Fragments can be any type of S6 Fragments.
  • the S6 Fragments are preferably
  • the S6 Fragments are preferably
  • the S6 Fragments can be preferably
  • the S6 Fragment is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoe
  • the S6 in Fragment is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoe
  • R 8 in the S6 is methyl.
  • the S is S6':
  • Fragment is
  • the S is -X-S6', and the structure of S6' is as described above;
  • X is O, NH or S, preferably O.
  • the S is S6a:
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6.
  • R 1 is hydrogen;
  • R 2 is selected from -O(C 1 -C 4 alkyl);
  • R 3 is hydrogen;
  • R 4 is C 1 - C 4 haloalkyl;
  • R 5 is selected from -NH 2 ;
  • R 7 is selected from C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.
  • the S is S6b:
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S is S6c:
  • R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S is -X-S6c, and the structure and definition of S6c are as described above; wherein, X is O, NH or S, preferably O.
  • the S is S6d:
  • X is O, NH or S, preferably O;
  • R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S6 is a specific compound of I-1 to I-383 in WO2018115380A1 (the entirety of which is incorporated herein by reference).
  • the S is S6e:
  • R 2 , R 3 and R 7 are as defined and described in any one of the schemes of S6.
  • the S is -X-S6e, and the structure and definition of S6e are as described above; wherein, X is O, NH or S, preferably O.
  • R 2 is -O(C 1 -C 4 alkyl); R 3 is hydrogen; R 7 is C 1 -C 6 alkyl.
  • R 2 is -OCH 3 ;
  • R 3 is hydrogen;
  • R 7 is methyl.
  • the S6, S6', S6a or S6c is any of the following structures:
  • the S6, S6', S6a, S6c or S6e are identical to each other.
  • the S is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl
  • S6 is S6 ":
  • R 1 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined and described in S6.
  • Fragment is
  • the S is -X-S6"', and the structure of S6"' is as described above; wherein X is O, NH or S, preferably O.
  • the S6" is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl
  • the S is S6a":
  • R 1 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6.
  • the S is S6b":
  • R 1 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S is S6c":
  • R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S is -X-S6c", and the structure and definition of S6c" are as described above; wherein, X is O, NH or S, preferably O.
  • the S is S6d":
  • X is O, NH or S, preferably O;
  • R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
  • the S is S6e":
  • the S is -X-S6e", and the structure and definition of S6e" are as described above; wherein, X is O, NH or S, preferably O.
  • R 3 is hydrogen; R 7 is C 1 -C 6 alkyl.
  • R 3 is hydrogen; R 7 is methyl.
  • the S6", S6"', S6a", S6c" or S6e" are identical to each other.
  • the S is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl
  • the S is
  • the S is
  • L is a bond
  • L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, - O-, -S-, -S(O)-, -S(O)NR 3' -, -NR 3' S(O)-, -S(O) 2 -, -S(O) 2 NR 3 ' -, -NR 3' S(O) 2 -, -NR 4' S(O) 2 NR 3' -, -CR 1' R 2' -, -C(O)-, -C(O)O -, -OC(O)-, -NR 3' C(O)O-, -OC(O)NR 3' -, -C(O)NR 3' -, -NR 3' C(O)NR 3' -, -NR 3' C(O)NR 3' -, -NR 3' C(
  • L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, -O-, -CR 1' R 2' -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O) -, -C(O)NR 3' -, -NR 3' C(O)-, -S(O) 2 NR 3' -, -NR 3' S(O) 2 -, vinylidene, acetylene base, phenyl, 8-10 membered bicyclic arylene, 3-7 membered saturated or partially unsaturated cycloalkylene, 5-11 membered saturated or partially unsaturated spirocycloalkylene, 5-11 membered Saturated or partially unsaturated fused
  • L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, -O-, -CR 1' R 2' -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O) -, -C(O)NR 3' -, -NR 3' C(O)-, -S(O) 2 NR 3' -, -NR 3' S(O) 2 -, vinylidene, acetylene base, phenyl, 8-10 membered bicyclic arylene, 3-7 membered saturated or partially unsaturated monocyclic cycloalkylene, 5-11 membered saturated or partially unsaturated spirocycloalkylene, 5- 11-membered saturated or partially unsaturated fuse
  • L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from the group consisting of -NH-, -NCH3-, -O-, -C( CH3 ) 2- , -CHF-, -CHCF3- , -C(O)-, -C(O)O- , -OC(O)-, -C(O)NH-, -C(O)NCH 3 -, -NHC(O)-, -NCH 3 C(O)-, vinylidene, ethynylene, Cyclopropyl, cyclobutylene, cyclopentylene, cyclohexylene, oxiranylene, oxetylene, oxolane, oxane, aziridine base, azetidine, azetidine, piperid
  • L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from the group consisting of -NH-, -NCH3-, -O-, -C( CH3 ) 2- , -CHF-, -CHCF3- , -C(O)-, -C(O)O- , -OC(O)-, -C(O)NH-, -C(O)NCH 3 -, -NHC(O)-, -NCH 3 C(O)-, cyclopropylene, cyclobutylene , cyclopentylene, cyclohexylene, oxane, oxetylene, oxolane, oxane, aziridine, aziridine , nitrosyl, piperidinide, piperazinide, morpholinide,
  • L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from -O-, -NH-, -NCH3-, -C(O)-, -C(O)NH-, -NHC(O) - , -NCH3C (O)-, - C(O)NCH 3 -, cyclohexylene, azidopropyl, azidobutyl, azidopentyl, piperidinylene, piperazinylene, group substitution, j is 4, 5, 6, 7, 8, 9 or 10.
  • L is selected from -(CH 2 ) j-1 -C(O)-, the methylene group in the -(CH 2 ) j-1 -C(O)- as defined in L above, optionally substituted by one or more groups, and said j is as defined in L above.
  • L is selected from
  • the L is any of the following structures:
  • the L is LA
  • Ring A is a bond, C 3 -C 12 cycloalkylene (eg wherein the a-terminus is attached to S and the b-terminus is attached to X"') or a 3-12 membered heterocycloalkylene group containing 1-2 heteroatoms selected from N, O or S (e.g.
  • the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxy, C 1 -C 6 Substituent substitution of alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
  • Ring B is a bond, C 3 -C 12 cycloalkylene (eg, wherein the c-terminus is attached to X"' and the d-terminus is attached to L3) or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S (eg wherein the c-terminus is attached to X"' and the d - terminus is attached to L3), the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxyl, C1 -C Substituent substitution of 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
  • Ring C is C 3 -C 12 cycloalkylene (eg wherein the e-terminus is attached to L and the f-terminus is attached to X”) or a 3-12 membered heterocycloalkylene group containing 1-2 heteroatoms selected from N, O or S (e.g.
  • the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxyl, C1 - C6 Substituent substitution of alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
  • L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally selected from -O-, -NH-, -C ⁇ C-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -C(O)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 -C 8 cycloalkane base)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
  • Ring A is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
  • Ring B is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
  • Ring C is C 3 -C 12 cycloalkylene or 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, said cycloalkylene and heterocycloalkylene is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 -C 6 alkyl) substituent substitution;
  • L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally selected from -O-, -NH-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 -C 8 cycloalkyl)- substitution, k is 0, 1, 2, 3 or 4;
  • L 3 is -(CH 2 ) k , and one or two methylene groups in the L 3 are optionally selected from -O-, -NH-, -C ⁇ C-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 - C8cycloalkyl )-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7.
  • ring A is a bond.
  • ring A is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms
  • ring A is a 3-6 membered saturated cycloalkylene group or a 4-7 membered saturated cycloalkylene group with one or two nitrogen heteroatoms independently selected from nitrogen heteroatoms.
  • Monocyclic heterocycloalkylene is a 3-6 membered saturated cycloalkylene group or a 4-7 membered saturated cycloalkylene group with one or two nitrogen heteroatoms independently selected from nitrogen heteroatoms.
  • ring A is a cyclohexylene group (such as cyclohexylene-1,4-diyl, such as trans-cyclohexylene-1,4-diyl), a piperidinyl (eg piperidine-1,4-diyl) or piperazinylene (eg piperazine-1,4-diyl).
  • cyclohexylene group such as cyclohexylene-1,4-diyl, such as trans-cyclohexylene-1,4-diyl
  • piperidinyl eg piperidine-1,4-diyl
  • piperazinylene eg piperazine-1,4-diyl
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • ring B is a bond.
  • ring B is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms
  • ring B is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, containing 1 or 2 nitrogens 7- to 11-membered spiroheterocycloalkylene or fused heterocycloalkylene of heteroatoms.
  • ring B is a piperidinide group (such as piperidine-1,4-diyl) or a piperazinide group (such as piperazine-1,4-diyl) base).
  • ring B is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • ring B is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • ring C is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms
  • ring C is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, containing 1 or 2 nitrogens 7- to 11-membered spiroheterocycloalkylene or fused heterocycloalkylene of heteroatoms.
  • ring C is a piperidinide group (such as piperidine-1,4-diyl), a piperazinide group (such as piperazine-1,4-diyl) base), (E.g ), (E.g ), (E.g ), (E.g ), (E.g ), (E.g ), (E.g )or (E.g ).
  • a piperidinide group such as piperidine-1,4-diyl
  • a piperazinide group such as piperazine-1,4-diyl
  • ring C is The e end is connected to L 3 and the f end is connected to X".
  • ring C is The e end is connected to L 3 and the f end is connected to X".
  • X" is a bond or -C(O)-.
  • X is a bond.
  • X" is -C(O)-.
  • X" is -C(O)CH 2 O-.
  • X"' is a bond or -C(O)-.
  • X"' is a bond.
  • X"' is -C(O)-.
  • k is 1, 2, 3, 4 or 5.
  • L 3 is -(CH 2 ) k
  • k is 1, 2, 3, 4 or 5.
  • L 3 is -(CH 2 ) k , and one or two methylene groups in the L 3 are optionally -O-, -NH- , -C ⁇ C- or -N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-) substitution, and k is 1, 2, 3, 4 or 5.
  • k is 1, 2, 3 or 4.
  • L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently optionally -O -, -NH- or -N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-) is replaced, or one -CH 2 CH 2 - contained in said L 3 is optionally - C ⁇ C-substitution; k is 1, 2, 3, or 4.
  • L 3 is -(CH 2 ) k -, and a methylene group in the L 3 is optionally -O-, -NH- or - Group substitution of N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-); k is 1, 2, 3 or 4.
  • the LA is LA-1:
  • Ring A , Ring B, Ring C, L3, X are as defined and described in LA.
  • the LA is LA-2:
  • ring A is wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
  • X"' is -C(O)-
  • Ring B is wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
  • L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in said L 3 are each independently optionally -O-, -NH- or -N(C 1 -C 6 alkyl )- (eg -N(CH 3 )-) is replaced, or one -CH 2 CH 2 - contained in the L 3 is optionally replaced by -C ⁇ C-; k is 1, 2, 3 or 4;
  • Ring C is Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
  • X" is -C(O)-.
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • ring B is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently any Optionally replaced by -O-, -NH- or -N( CH3 )-; k is 1, 2, 3 or 4.
  • L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently any Selected is replaced by -O-; k is 1, 2, 3 or 4.
  • k is 3 or 4, preferably 4.
  • L 3 is -(CH 2 ) k -, wherein one CH 2 contained in the L 3 is optionally -O- substitution; k is 4.
  • L 3 in the LA, LA-1 and LA-2, L 3 can be -CH 2 -, -(CH 2 ) 2 -, -(CH 2 ) 3 -, -(CH 2 ) 4- ,
  • the k" end is connected to ring B, and the k' end is connected to ring C.
  • L 3 in the LA, LA-1 and LA-2, L 3 can be -(CH 2 ) 4 -,
  • ring C is The e end is connected to L 3 and the f end is connected to X".
  • the LA-2 is any of the following structures:
  • the LA-2 is any of the following structures:
  • the LA is LA-3:
  • ring A is wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
  • X"' is -C(O)-
  • Ring B is wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
  • L 3 is -(CH 2 ) k -, wherein one CH 2 contained in said L 3 is optionally -O-, -NH- or -N(C 1 -C 6 alkyl)- (eg -N (CH 3 )-) substitution; k is 1 or 2;
  • Ring C is Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
  • X" is -C(O)-.
  • ring A is preferably The a-end is connected to S, and the b-end is connected to X"'.
  • ring B is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • L 3 is -(CH 2 ) k -, and k is 1 or 2.
  • ring C is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • the LA-3 is any of the following structures:
  • the LA-3 is any of the following structures:
  • the LA is LA-4:
  • ring A is wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
  • X"' is a bond, -C(O)NH- or -C(O)NCH 3 -;
  • Ring B is a bond
  • L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally -O-, -NH-, -C(O)-, -C ⁇ C- or -N (C 1 -C 6 alkyl)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
  • Ring C is Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
  • X" is -C(O)-.
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • L 3 is -CH 2 -,
  • the k" end is connected to ring B, and the k' end is connected to ring C.
  • ring C is The e end is connected to L 3 and the f end is connected to X".
  • the LA-4 is any of the following structures:
  • the LA-4 is any of the following structures:
  • the LA is LA-5:
  • Ring A, X''', Ring B, L 3 and Ring C are as defined in LA-2 or LA-3;
  • X" is -C(O)CH 2 O-, and -C(O)- in X" is connected to ring C.
  • ring A is The a-end is connected to S, and the b-end is connected to X"'.
  • ring B is Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
  • L 3 is -(CH 2 ) k , and k is 1 or 2, preferably 1.
  • ring C is The e end is connected to L 3 and the f end is connected to X".
  • the LA-5 is N-(2-aminoethyl)-2-aminoethyl
  • the LA is a first polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization polarization
  • the E is a small molecule ligand of CRBN, VHL, XAIP or MDM2E3 ubiquitin ligase.
  • the E is E1, E1a, E1b or E1c
  • Each R is independently halogen , optionally substituted acyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocycle, optionally substituted heterocycle , optionally substituted aryl, optionally substituted heteroaryl, -CN or -O(CH 2 ) X R 1A ;
  • R 1 is -O(CH 2 ) x R 1A ;
  • R 6 is unsubstituted isopropyl, -(CH 2 )C(O)OMe, or -(CH 2 ) 2 OH;
  • R 6A is substituted alkyl
  • R 7 is hydrogen, optionally substituted acyl, optionally substituted alkyl, or nitrogen protecting group
  • R 1A is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocycle, optionally substituted heterocycle, optionally substituted aryl, optionally substituted of heteroaryl, -OR A , -N(R B ) 2 , or -SR A ;
  • Each R A is independently hydrogen, optionally substituted acyl, optionally substituted alkyl, and when attached to O is an oxygen protecting group and when attached to S is a sulfur protecting group;
  • each R is independently hydrogen, optionally substituted acyl, optionally substituted alkyl, nitrogen protecting group;
  • n 1, 2, 3, or 4;
  • x is 0, 1, 2, 3, 4, 5, or 6 , and when R6 is isopropyl, R6A is methyl, R7 is hydrogen, and n is 1 , R1 is not methyl or hydroxymethyl .
  • the E is E2
  • X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
  • X 201 is C or Si
  • X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
  • R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
  • R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP( O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N(R 100 ) 2 ], -OP(O)[N(R 100 ) 2 ]
  • Ring A is bicyclic or tricyclic, selected from
  • Ring B is a 6-membered heteroaryl group containing 1-2 N atoms, a phenyl group, a 5-7 membered saturated or partially unsaturated cycloalkyl group, a group containing 1-2 heteroatoms selected from N, O, and S. 5-7-membered saturated or partially unsaturated heterocycloalkyl, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, and S;
  • R 301 is selected from hydrogen, halogen, -OR 100 , -SR 100 or -N(R 100 ) 2 ;
  • R 401 is hydrogen, -R 601 , -halogen, -CN, nitro, -OR 100 , -SR 100 , -N(R 100 ) 2 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 or -NR 100 S(O) 2 R 100 ;
  • R 501 is hydrogen, -CN or C 1 -C 4 alkyl
  • R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
  • R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 saturated or partially unsaturated 4-7 membered heteroaryl groups selected from N, O or S heteroatoms;
  • n 0, 1, 2, 3 or 4.
  • E is E3:
  • X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
  • X 201 is C, N or Si
  • X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
  • R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
  • Ring A is absent or monocyclic or bicyclic, selected from:
  • R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC( O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP(O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N
  • Ring B is a 6-membered heteroaryl group containing 1-2 N atoms, a phenyl group, a 5-7 membered saturated or partially unsaturated cycloalkyl group, a group containing 1-2 heteroatoms selected from N, O, and S. 5-7-membered saturated or partially unsaturated heterocycloalkyl, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, and S;
  • R 301 and R 401 are each independently hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , - N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 or -NR 100 S(O) 2 R 100 ;
  • R 501 is hydrogen, -CN or C 1 -C 4 alkyl
  • R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
  • R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 heteroatoms selected from N, O or S;
  • P" is 0 or 1
  • n 0, 1 or 2;
  • n" 0, 1, 2, 3 or 4.
  • E is E4:
  • X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
  • X 201 is C, N or Si
  • X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
  • R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
  • R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC( O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP(O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N
  • R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
  • R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 heteroatoms selected from N, O or S;
  • Ring E, Ring F and Ring G are each independently a 6-membered heteroaryl containing 1-2 N atoms, a phenyl, a 5-7 membered saturated or partially unsaturated cycloalkyl, containing 1-2 optional 5-7-membered saturated or partially unsaturated heterocycloalkyl from N, O, S heteroatoms, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, S;
  • m" is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16.
  • E is E5:
  • ring M is selected from or
  • Each of X 101 , X 601 and X 701 is independently a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P(O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
  • Each X 301 and X 501 is independently a bond, -C(R 100 ) 2 -, -NR 100 -, -O-, -S-, or -Si(R 100 ) 2 -;
  • Each R 100 is independently selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially containing 1-2 heteroatoms selected from N, O or S Unsaturated heterocycloalkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O, or S, or two R 100 together with the N atom to which it is attached form except the one to which the N atom is attached. Also contains 0-3 heteroatoms selected from N, O or S;
  • Each R 301a is independently hydrogen, deuterium, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -N(R 100 ) 2 , -Si(R 100 ) 3 , - S(O)R 100 , -S(O) 2 R 100 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O) N(R 100 ) 2 , -C(O)N(R 100 )OR 100 , -C(R 100 ) 2 N(R 100 )C(O)R 100 , -C(R 100 ) 2 N(R 100 )C(O)N(R 100 ) 2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)OR
  • Each R 601 is independently optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heteroatoms containing 1-2 heteroatoms selected from N, O or S. Cycloalkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S;
  • Each R 701 is independently hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O)(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 )-, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C1-C4 alkyl; or
  • R 701 and X 101 or X 301 together with the atoms to which they are attached form a 5-7 membered saturated or partially unsaturated carbocyclic ring or a heterocyclic ring containing 1-3 heteroatoms selected from boron, N, O, Si or S ;
  • R 701 on the same carbon together with the atoms to which they are attached form a 3-6 membered ring or a 4-7 membered heterocycle containing 1-2 heteroatoms selected from boron, N, O, Si or S;
  • R 701 on adjacent carbons together with their attached atoms form a 3-7 membered saturated or partially unsaturated carbocyclic ring or a heteroatom containing 1-3 heteroatoms selected from boron, N, O, Si or S ring, or form a saturated or partially unsaturated 7-13 membered bridged heterocycle or spiro heterocycle containing 1-3 heteroatoms selected from boron, N, O, Si or S;
  • Ring D is each independently a 6-membered heteroaryl, phenyl, 5-7 membered saturated or partially unsaturated cycloalkyl containing 1-4 heteroatoms selected from N, O or S heteroatoms, containing 1-3 5-7-membered saturated or partially unsaturated heterocycloalkyl selected from N, O, S heteroatoms, or 5-membered heteroaryl containing 1-4 heteroatoms selected from N, O, S;
  • n" is 0, 1, 2, 3 or 4;
  • q" is 0, 1, 2, 3 or 4.
  • E is E6, E6a, E6b, E6c, E6d, E6e, E6f, E6g, E6h or E6i:
  • Y is a bond, Y 1 , O, NH, NR 2 , C(O)O, C(O)NR 2 ', Y 1 -O, Y 1 -NH, Y 1 -NR 2 , Y 1 -C(O ), Y1-C(O)O, Y1 -OC(O), Y1 -C(O)NR2' or Y1 - NR2'C (O), wherein Y1 is C1 - C6 sub alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl;
  • X is C(O) or C(R 3 ) 2 ;
  • each R 1 is independently halogen, nitro, NH 2 , OH, C(O)OH, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • R 2 is C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl or C(O)-3-8 membered heterocycloalkyl , and R 2 can be optionally selected by one or more of halogen, N(R a ) 2 , NHC(O)R a , NHC(O)OR a , OR b , C 3 -C 8 cycloalkyl, 3- 8-membered heterocycloalkyl, C 6 -C 10 -membered aryl, or 5-10-membered heteroaryl, wherein C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, C 6 -C 10 -aryl or 5-10 membered heteroaryl can be optionally replaced by one or more halogen, NH2 , CN, nitro, OH, C(O)OH, C1 - C
  • R 2 ′ is H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 8 cycloalkyl or 3-8-membered heteroheterocycloalkyl, and when R 2 ′ is not H , which can be optionally replaced by one or more halogens, N(R a ) 2 , NHC(O)R a , NHC(O)OR a , OR b , C 3 -C 8 cycloalkyl, 3-8 membered hetero substituted by cycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl, wherein C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, C 6 -C 10 aryl or 5 -10 membered heteroaryl can be optionally substituted by another one or more halogen, NH2 , CN, nitro, OH, C(O)OH, C1 - C6 al
  • each R is independently H or C 1 -C 3 alkyl optionally substituted with C 6 -C 10 aryl or 5-10 membered heteroaryl ;
  • each R 3 ' is an independent C 1 -C 3 alkyl
  • Each R 4 is independently H or C 1 -C 3 alkyl; or two R 4 together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl or contain 1 or 2 optional 4-, 5- or 6-membered heterocycloalkyl from heteroatoms of N and O;
  • R 5 is H, C 1 -C 3 alkyl, F or Cl;
  • each R is independently H or C 1 -C 6 alkyl ;
  • R b is H or tosyl
  • t is 0 or 1;
  • n 0, 1, 2 or 3;
  • n 0, 1 or 2.
  • Rings A, X, X 1 , X 2 , Y 100 , R 1 , R 3 , R 3′ , R 4 , R 5 , t, m and n are as defined in WO2017/007612 and US2018/0134684, and through in their entirety Incorporated herein by reference.
  • E is E7, E7b, E7c, E7d or E7e:
  • W is CH 2 , CR a R b , C(S), C(O) or SO 2 ;
  • X is H 2 , CH 2 , O or S
  • Y is NH, N-alkyl, N-aryl, N-heteroaryl, N-cycloalkyl, N-heterocycloalkyl, O or S;
  • Z is H 2 , CH 2 , O or S, and in E7c, Z cannot be H 2 at the same time;
  • G and G' are each independently selected from hydrogen, C1 - C6 alkyl, OH, -CH2 -heterocycloalkyl optionally substituted with R ' , -CH2 -phenyl optionally substituted with R ' ;
  • Q 1 , Q 2 , Q 3 and Q 4 are each independently carbon, nitrogen or nitrogen oxides
  • A is hydrogen, C 1 -C 6 alkyl, cycloalkyl or halogen
  • R, R a and R b are each independently selected from hydrogen, hydroxy, halogen, -NH 2 , -N(C 1 -C 6 alkyl) 1-2 , C 1 -C 6 alkyl, C 1 -C 6 Alkoxy, C 1 -C 6 haloalkyl, -CONR ' R", -OR ' , -NR ' R", -SR ' , -SO 2 R ' , -SO 2 NR ' R", -CR ' R ", -CR ' NR ' R ", aryl, heteroaryl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, -P(O)(OR ' )R", -P( O) R'R", -OP(O)(OR' ) R", -Cl, -F, -Br, -I, -CF3 , -CN, -NR'SO2NR'
  • R ' and R" are each independently selected from bond, hydrogen, C1 - C6 alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl;
  • n" is an integer from 1 to 4.
  • ----- is a bond, which may be an R stereoisomer, an S stereoisomer, or a non-stereoisomer.
  • E is:
  • E is E8, E8a, E8b, E8c, E8d, E8e, E8f, E8g, E8h, E8i, E8j, E8k, E8l, E8m, E8n, E8o, E8p, E8q, E8s, E8t, E8u , E8v, E8w, E8x, E8y, E8z, E8aa, E8bb or E8cc:
  • Each W is independently selected from CH 2 , CHR, C(O) or SO 2 ;
  • Q 1 , Q 2 , Q 3 , Q 4 , Q 5 are each independently carbon, N, or N substituted by R', or nitrogen oxides;
  • R 1 is absent or is hydrogen, hydroxyl, cyano, C 1 -C 3 alkyl or C(O);
  • R 2 is absent, or is hydrogen, hydroxyl, cyano, C 1 -C 3 alkyl, CHF 2 , CF 3 , CHO or C(O)NH 2 ;
  • R 3 is selected from hydrogen, alkyl (eg: C 1 -C 6 alkyl or C 1 -C 3 alkyl), optionally substituted alkyl (eg: C 1 -C 6 alkyl or C 1 -C 3 alkyl), alkoxy (such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy), optionally substituted alkoxy (such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy);
  • alkyl eg: C 1 -C 6 alkyl or C 1 -C 3 alkyl
  • alkoxy such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy
  • optionally substituted alkoxy such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy
  • R4 is selected from hydrogen, alkyl or optionally substituted alkyl
  • R 5 or R 6 are each independently selected from hydrogen, halogen, C(O)R', cyano, hydroxyl, CF 3 ;
  • X is carbon, nitrogen or C(O);
  • X 1 is carbon, nitrogen or C(O);
  • R' is selected from hydrogen, halogen, amine, alkyl (eg: C 1 -C 3 alkyl), optionally substituted alkyl (eg: C 1 -C 3 alkyl), alkoxy (eg: C 1 -C 3 alkoxy), optionally substituted alkoxy (eg: C 1 -C 3 alkoxy), NR 2 R 3 , C(O)OR 2 , optionally substituted phenyl;
  • R is H, OH, lower alkyl, lower alkoxy, cyano, halogenated lower alkoxy or halogenated lower alkyl;
  • n 0, 1, 2, 3 or 4;
  • E is E9a, E9b, E9c, E9d, E9e, E9f, E9g, E9h, E9i, E9j, E9k, E9l, E9m, E9n, E9o, E9p, E9q, E9r, or E9s:
  • R 1 is selected from H, CN, C 1 -C 3 alkyl
  • R 2 is H or C 1 -C 3 alkyl
  • R 4 is methyl or ethyl
  • R 5 is H or halogen
  • R 6 is H or halogen
  • R is H
  • R' is H
  • Q 1 and Q 2 are each independently C or N substituted with a group independently selected from H or C 1 -C 3 alkyl;
  • E is E10, E10a or E10b:
  • the X A is C(O) or C(R 3A ) 2 ;
  • Z is NR 3A or CR 3A ;
  • Each R 1A is independently halogen, hydroxy, -C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • Each R 3A is independently hydrogen or C 1 -C 3 alkyl
  • R 3' is each independently C 1 -C 3 alkyl
  • Each R 4A is independently hydrogen or C 1 -C 3 alkyl, or two R 4A together with the carbon atom to which they are attached form C(O), C3-C6 cycloalkyl, or together form a C(O), C3-C6 cycloalkyl group containing 1 or 2 3-membered, 4-membered, 5-membered or 6-membered heterocycloalkyl selected from N or O heteroatoms;
  • R 5A is selected from hydrogen, C 1 -C 3 alkyl or halogen
  • Each R 6A is independently hydrogen or C 1 -C 3 alkyl, or two R 6A together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl, or together form a C(O), C 3 -C 6 cycloalkyl group containing 1 one or two 3-, 4-, 5- or 6-membered heterocycloalkyls selected from N or O heteroatoms;
  • n 0, 1, 2 or 3;
  • n 0, 1 or 2;
  • a1 is 0 or 1.
  • E is E11:
  • Each R 1A is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • R 3A is hydrogen or C 1 -C 3 alkyl
  • R 3' is each independently C 1 -C 3 alkyl
  • R 4A is hydrogen, or C 1 -C 3 alkyl; or two R 4A together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl, or together form a cycloalkyl containing 1 or 2 4-membered, 5-membered or 6-membered heterocycloalkyl selected from N or O heteroatoms;
  • n 0, 1, 2 or 3;
  • n 0, 1 or 2;
  • a1 is 0 or 1.
  • E is E12:
  • Each R 2' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • Each R 4' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • Each R 5' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • n1 0, 1, 2, 3, 4, 5 or 6;
  • n2 is 0, 1, 2, 3 or 4;
  • n3 0, 1 or 2.
  • E is E13:
  • R 3A is hydrogen, or C1-C3 alkyl
  • each R 3' is C 1 -C 3 alkyl
  • Each R 6' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
  • n1 0, 1, 2, 3, 4 or 5;
  • n1 0, 1, 2, 3, 4, or 5.
  • E is E14, E14a, E14b, E14c, E14d or E14e:
  • Ar is aryl, cycloalkyl, heterocycloalkyl or heteroaryl
  • R', R", R"' are each independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted ether, substituted or unsubstituted cycloalkyl, substituted or unsubstituted or unsubstituted heterocycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted Heteroalkyl, substituted or unsubstituted alkylated acylaryl, or substituted or unsubstituted amine; r is an integer from 1 to 6;
  • R 1 , R 2 , R 3 are each independently selected from H, halogen, hydroxyl, azide, alkoxy, mercapto, imino, amino, phosphonate, phosphate, carbonyl, carboxyl, cyano, silane group, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, substituted or unsubstituted amine, substituted or unsubstituted amide, nitro, ester, morpholinyl, dioxolane, substituted or unsubstituted substituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted or unsubstitute
  • R 1 and R 2 combine to form a 5-7 membered heterocycle, and when R 1 and R 2 combine to form a 5-7 membered heterocycle, Ar and the 5-7 membered heterocycle do not form a combined ring, but a 5-7 membered heterocycle. Substituents of membered heterocycles;
  • R 4 , R 5 are hydrogen, halogen, hydroxyl, azide, ether, alkoxy, mercapto, alkylthio, sulfonyl, sulfonamide, ketone, aldehyde, ester, substituted or unsubstituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenone, unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocycle base or a combination thereof;
  • R 8 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, or a combination thereof;
  • x 0, 1 or 2;
  • y is an integer from 1 to 6.
  • Ring B is aryl, heteroaryl, cycloalkyl, heterocycloalkyl;
  • L 101 is a bond or C 1 -C 6 alkyl
  • A is C, S, substituted or unsubstituted C 1 -C 8 alkyl or a combination thereof;
  • G 100 is C, S, N, substituted or substituted C 1 -C 8 alkyl or a combination thereof;
  • R 101 , R 201 and R 301 are independently selected from hydrogen, halogen, hydroxyl, azide, alkoxy, mercapto, imino, amido, phosphonate, phosphinate, carbonyl, carboxyl, cyano, methyl Silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, substituted or unsubstituted amine, substituted or unsubstituted amide, nitro, ester, morpholino, dioxolane, substituted or unsubstituted alkyl, substituted or unsubstituted alkyl halide, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl , substituted or unsubstituted cycloalky
  • R 401 and R 501 are independently selected from hydrogen, halogen, hydroxyl, azide, ether, alkoxy, mercapto, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, substituted or unsubstituted alkyl , substituted or unsubstituted alkyl halides, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocycloalkyl and its combination;
  • R 601 and R 701 are each independently oxo, hydrogen, C 1 -C 8 alkyl, or R 601 and R 701 combine together to form oxo;
  • R 801 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyl halide, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted or unsubstituted cycloalkyl, heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkaryl, and combinations thereof;
  • x" and y" are independently 0, 1 or 2;
  • E is E16, E16a or E16b:
  • X 100 is independently selected from NH, NR 301 , CH 2 , CHR 301 , C(R 301 ) 2 , O or S;
  • n" 0, 1, 2 or 3;
  • n" is 0, 1, 2 or 3; when When it is a double bond, n" is 0, 1 or 2;
  • R 101 is selected from:
  • R 201 is alkyl, hydrogen, heteroalkyl, aryl, heteroaryl or heterocycloalkyl
  • R 101 and R 201 combine to form a 4, 5, 6, 7, 8, 9 or 10-membered heterocycloalkyl or heteroaryl, which is optionally selected by one or more Substituted from the substituents of R 501 and R 120 ;
  • R 101* is selected from:
  • R 301 is selected from: alkyl, -C(O)H, C(O)OH, -C(O) alkyl, -C(O)O alkyl, alkenyl, alkynyl, aryl, heteroaryl or heteroalkyl;
  • R 401 is selected from alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, cyano, -NH(alkyl), -N(alkyl) 2 , -NHS(O) 2 (alkyl), -N(alkyl)SO 2 alkyl, -NHSO 2 (aryl, heteroaryl or heterocycloalkyl), -N(alkyl)SO 2 (aryl, heteroaryl or Heterocycloalkyl), -NHSO 2 (alkenyl), -N(alkyl)SO 2 (alkenyl), -NHSO 2 (alkynyl), -N(alkyl)SO 2 (alkynyl), or haloalkyl , aryl, heteroaryl, heteroalkyl and cycloalkyl;
  • R 501 and R 140 are each independently selected from hydrogen, alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, cyano, -NH(alkyl), -N(alkyl ) 2 , -NHS(O) 2 (alkyl), -N(alkyl)SO 2 (alkyl), -NHSO 2 (aryl, heteroaryl or heterocycloalkyl), -N(alkyl) SO 2 (aryl, heteroaryl or heterocycloalkyl), -NHSO 2 (alkenyl), -N(alkyl)SO 2 (alkenyl), -NHSO 2 (alkynyl), -N(alkyl) ) SO 2 (alkynyl) or haloalkyl, aryl, heteroaryl, heteroalkyl and cycloalkyl;
  • R 501 is independently selected from C(O)R 401 , cyano, aryl, aryloxy, heterocycloalkyl, heteroaryl, arylalkyl, alkoxy, hydroxy, O-aralkyl or cycloalkyl;
  • R 601 , R 701 , R 801 , R 901 , R 1001 , or R 110 are independently selected from hydrogen, alkyl, heteroalkyl, hydroxy, alkoxy, amine, -NH(alkyl), and -N(alk base) 2 ;
  • R 601 and R 701 together with the carbon atom to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle, or a 4, 5, or 6-membered ring containing 1 or 2 heteroatoms selected from N, O Spiroheterocycle;
  • R 801 and R 901 together with the carbon atoms to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle; or form a 4, 5, or 6-membered ring containing 1 or 2 heteroatoms selected from N, O Spiroheterocycle;
  • R 1001 and R 110 together with the carbon atom to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle; Spiroheterocycle;
  • R 601 and R 801 together form 1 or 2 carbon bridged rings
  • R 601 and R 1001 together form 1 or 2 carbon bridged rings
  • R 801 and R 1001 together form 1 or 2 carbon bridged rings
  • R 601 and R 140 together form a 3, 4, 5 or 6 carbon fused ring
  • R 140 and R 1001 together form a 3, 4, 5 or 6 carbon fused ring
  • R 801 and R 140 together form 1 or 2 carbon bridged rings
  • R 401 and R 140 together form a 3, 4, 5 or 6 carbon fused ring, wherein said R 501 is located on the alpha carbon of R 140 , or together form 1, 2, 3 or 4 carbon bridged rings, wherein said R 501 Said R 501 is not located on the R 140 alpha carbon;
  • R 120 is L 100 ;
  • R 170 is selected from:
  • Y 100 is selected from N, CH or CR 101 ; wherein 0, 1, 2 or 3 Y 100 are N;
  • R 101 is independently selected from hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, hydroxy, aryl, heteroaryl, heterocycloalkyl, aralkyl, heteroaralkyl, heterocycloalkane group, aryloxy, heteroaryloxy, CN, -C(O)O alkyl, -C(O)OH, NO 2 , F, Cl, Br, I, CF 3 , NH 2 , NH(alkyl ), N(alkyl) 2 , or heteroalkyl.
  • E is E17, E17a, E17b or E17c:
  • X and X 1 are each independently selected from NH, NR 3 , CH 2 , CHR 3 , C(R 3 ) 2 , O or S;
  • n" 0, 1, 2 or 3;
  • n" is 0, 1, 2 or 3; When it is a double bond, n" is 0, 1 or 2;
  • R1 is or R 1* , where X is O or N, and when X is O oxygen, R 2 is absent;
  • Ring A is phenyl, 5-6 membered heteroaryl, 3-6 membered cycloalkyl or 4-6 membered heterocycloalkyl, said phenyl, 5-6 membered heteroaryl, 3-6 membered cycloalkane radical or 4-6 membered heterocycloalkyl optionally substituted by R 12 ;
  • Ring B is absent, phenyl or 5-6 membered heteroaryl optionally substituted by R 5 or R 12 ;
  • R 2 is alkyl, H, aliphatic, heteroaliphatic, aryl, heteroaryl or heterocycloalkyl;
  • R 1* is optionally substituted aryl, heteroaryl, cycloalkyl, heterocycloalkyl, alkylamino, alkoxy, ester, sulfonyl or amido;
  • R is alkyl, -C(O)H, -C(O)OH, -C(O)alkyl, -C(O)Oalkyl, alkenyl or alkynyl;
  • R 4 is alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, -NH alkyl, -N(alkyl) 2 , -NHSO 2 alkyl, -N(alkyl )SO 2 alkyl, -NHSO 2 aryl, -N(alkyl) SO 2 aryl, -NHSO 2 alkenyl, -N(alkyl) SO 2 alkenyl, -NHSO 2 alkynyl, -N(alk base) SO 2 alkynyl or halogenated alkane;
  • R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are independently selected from hydrogen, alkyl, aliphatic, heteroaliphatic, hydroxy, alkoxy, amine, -NH (aliphatic, including alkyl ) and -N (aliphatic, including alkyl) 2 ;
  • R 6 , R 7 and the carbon atoms to which they are bonded together form a 3-, 4-, 5- or 6-membered spirocarbocyclic ring, or a 4-, 5- or 6-membered spirocyclic heterocyclic ring, and the heteroatom is 1 or 2 N or O;
  • R 8 , R 9 and the carbon atoms to which they are bonded together form a 3, 4, 5 or 6-membered spirocarbocycle, or a 4, 5 or 6-membered spirocyclic heterocycle, and the heteroatom is 1 or 2 N or O;
  • R 10 , R 11 and the carbon atoms to which they are bonded together form a 3-, 4-, 5- or 6-membered spirocarbocyclic ring, or a 4-, 5- or 6-membered spirocyclic heterocycle, and the heteroatom is 1 or 2 N or O;
  • R 6 and R 8 form 1 or 2 carbon bridge rings
  • R 6 and R 10 form 1 or 2 carbon bridge rings
  • R 8 and R 10 form 1 or 2 carbon bridge rings
  • R 14 , R 6 form 3, 4, 5 or 6 carbon fused rings
  • R 14 and R 10 form 3, 4, 5 or 6 carbon fused rings
  • R 14 and R 8 form 1 or 2 carbon bridge rings
  • R 14 , R 4 form a 3, 4, 5 or 6 carbon fused ring, and R 4 is on the carbon ⁇ attached to R 14 or forms a 1, 2, 3 or 4 carbon bridged ring, and R 4 is not attached to R 14 on carbon ⁇ ;
  • R 12 is the chain connecting the target ligand
  • R 5 and R 14 are respectively selected from hydrogen, alkyl, alkene, alkyne, halogen, hydroxyl, alkoxy, azide, amino, cyano, -NH (aliphatic, including alkyl), -N (aliphatic) family, including alkyl) 2 , -NHSO 2 (aliphatic, including alkyl), -N (aliphatic, including alkyl) SO 2 alkyl, -NHSO 2 (aryl, heteroaryl or heterocycle), C(O)R 4 , -N(alkyl)SO 2 (aryl, heteroaryl or heterocycle), -NHSO 2 alkenyl, -N(alkyl) SO 2 alkenyl, -NHSO 2 alkynyl, -N(alkyl) SO2alkynyl , haloalkyl, aliphatic, heteroaliphatic, aryl, heteroaryl, heteroalkyl and carbocyclic;
  • each R5 may optionally be replaced by one or more selected from the group consisting of alkyl, alkene, alkyne, halogen, hydroxy, alkoxy, azide, amino, -NHalkyl, -N(alkyl) 2 , aryl, heterocycloalkyl, heteroaryl, haloalkyl and cycloalkyl;
  • R 1 , R 4 , R 10 , R 11 , R 14 , R 16 , W 1 , W 2 , X, and n are as defined in WO2018/237026, the entire contents of which are incorporated herein by reference.
  • X 1 is -C(R) 2 , -O-, -NR-, -CF 2 -, -C(O)-, -C(S)- or
  • X 2 and X 3 are each independently -CH 2 -, -C(O)-, -C(S)-, -C(R) 2 C(O)- or
  • Z 1 and Z 2 are each independently a carbon atom or a nitrogen atom
  • Ring A x is selected from phenyl, 4-6 membered saturated or partially unsaturated cycloalkyl or heterocycloalkyl containing 1-3 heteroatoms selected from N, O or S, 5-6 membered containing 1-4 heteroaryl groups selected from N, O or S heteroatoms;
  • Rx is selected from hydrogen, deuterium, -Rz , halogen, -CN, -NO2 , -OR, -SR, -N(R) 2 , -S(O)R, -S(O ) 2R, - S(O) 2 N(R) 2 , -CF(R) 2 -, -CF 2 R-, -CF 3 -, -C(R) 2 (OR)-, -C(R) 2 [N( R) 2 ]-, -C(O)R, -C(O)OR, -C(O)N(R) 2 , -C(O)N(R)OR, -OC(O)R, - OC(O)N(R) 2 , -C(S)NR 2 , -NRC(O)OR, -NRC(O)R, -NRC(O)N(R) 2 , -NRS(O)NR 2 , -NRC(
  • R x together with the atoms to which they are attached form an optionally substituted 5-8 membered partially unsaturated or aryl-fused heterocycloalkyl containing 0-2 heteroatoms selected from N, O or S;
  • Each R is independently hydrogen, or optionally substituted selected from C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated containing 1-2 members selected from N, O or Heterocycloalkyl with S heteroatom, 5-6 membered heteroaryl ring containing 1-4 heteroatoms selected from N, O or S; or
  • R y is selected from hydrogen or
  • Ring B x is selected from phenyl, 4-10 membered saturated or partially unsaturated monocyclic or bicyclic cycloalkyl or heterocycloalkyl containing 1-3 heteroatoms selected from N, O or S, or 5- 6-membered heteroaryl group containing 1-4 heteroatoms selected from N, O or S, and the ring B x is further optionally substituted by 1-2 oxo groups;
  • Each R w is independently selected from hydrogen, deuterated, R z , halogen, -CN, -NO 2 , -OR, -SR, -N(R) 2 , -S(O)R, -S(O ) 2 R, -S(O) 2 N(R) 2 , -CF(R) 2 -, -CF 2 R-, -CF 3 -, -C(R) 2 (OR)-, -C(R ) 2 [N(R) 2 ]-, -C(O)R, -C(O)OR, -C(O)N(R) 2 , -C(O)N(R)OR, -OC( O)R, -OC(O)N(R) 2 , -C(S)NR 2 , -NRC(O)OR, -NRC(O)R, -NRC(O)N(R) 2 , -NRS (O) 2 R, -C(
  • Each R z is independently C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, 5-6 membered heteroaryl rings containing 1-4 heteroatoms selected from N, O or S;
  • x 0, 1, 2, 3, or 4;
  • y 0, 1 or 2;
  • w 0, 1, 2, 3, or 4.
  • R 5 is H, methyl or F
  • R 16a , R 16b , R 16c and R 16d are each independently selected from H, halogen or C 1 -C 4 alkyl.
  • E19, E19a, E19b, E19c, E19d, E19e, E19f, E19g, E19h and E19i A 1 , A 2 , A 3 , Z, G and R 5 are as described in WO2017/176958 (which is hereby incorporated by reference in its entirety as defined and described in .
  • E is E20, E20a, E20b, E20c, E20d, E20e or E20f:
  • L1 is selected from : key
  • X 1 , X 2 , X 3 and X 4 are each independently selected from nitrogen or CR 4 , and at most two of X 1 , X 2 , X 3 and X 4 are simultaneously selected from nitrogen;
  • Z 2 and Z 3 are selected from -CH 2 - or -C(O)- and at least one of Z 1 and Z 2 is selected from -C(O)-;
  • o is selected from 0, 1, 2, 3 or 4;
  • Each R 4 is independently selected from hydrogen, halogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkyl;
  • Each R 5 is independently selected from hydrogen, C 1 -C 6 alkyl or -C(O)-alkyl;
  • Each R 8 is independently selected from hydrogen, C 1 -C 6 alkyl or C 1 -C 6 haloalkyl; or two R 8 together with the atom to which they are attached are cyclopropyl.
  • E is E21:
  • X" is C or N
  • Y" is C, N, O or S
  • Q 1 , Q 2 , Q 3 , Q 4 , Q 5 are independently CR 3 ′′ or N;
  • R 3 " is each independently hydrogen, deuterium, hydroxy, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl (eg morpholinyl ,E.g ), 6-10-membered aryl, 5-10-membered heteroaryl, -O(C 1 -C 6 alkyl), -O-(C 3 -C 8 cycloalkyl), -O-(3-8 membered heterocycloalkyl), N(C 1 -C 6 alkyl) 1-2 , NH(C 3 -C 8 cycloalkyl), NH(3-8 membered heterocycloalkyl), -O-(6 -10 aryl), -O-(5-10 membered heteroaryl); the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally selected by 1-3 independent Substitute
  • n 1, 2 or 3;
  • R 1 " is independently hydrogen, deuterium, hydroxyl, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, 6-10 membered Aryl, 5-10 membered heteroaryl, -O(C 1 -C 6 alkyl), the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally substituted by 1-3 substituted with groups independently selected from hydroxyl, halogen, cyano, amino;
  • R 2 " is hydrogen, deuterium, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, and the C 1 -C 6 alkyl and C 3 -C 6 cycloalkyl are optionally surrounded by 1-3 substituted with a group independently selected from hydroxy, halogen, cyano, amino.
  • one or two of Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 in the E21 are N, and the rest are independently CR 3 ′′.
  • Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 in the E21 are each independently CR 3 ′′.
  • X" in the E21 is N.
  • X" in the E21 is C.
  • Y" in the E21 is N.
  • each of R 1 " in the E21 is independently hydrogen, deuterium, -F, -Cl, or C 1 -C 6 alkyl, and the alkyl is optionally replaced by 1-3 Halogen substituted ; preferably R1" is hydrogen.
  • R 2 " in the E21 is hydrogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted with 1-3 halogens; preferably R 2 " is hydrogen.
  • R 3 " in the E21 is each independently hydrogen, deuterium, halogen, -O(C 1 -C 6 alkyl), or C 1 -C 6 alkyl, the alkane
  • the group is optionally substituted by 1-3 halogens; preferably R 3 " is independently hydrogen, deuterium, F, Cl, methyl, methoxy, ethoxy, trifluoromethoxy, 2-hydroxypropan-2 group or trifluoromethyl.
  • m in the E21 is 2.
  • the E21 has the following structure
  • the E21 has the following structure
  • the E21 has the following structure
  • said E21 has the following structure
  • said R 3 " is as defined in E21 above.
  • said E21 has the following structure
  • the E21 has the following structure
  • the E21 has the following structure
  • R 1 ", R 2 ", R 3 " are as defined in E21-1 above.
  • the E21 has the following structure
  • the E21 has the following formula:

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Abstract

An SOS1 degrading agent and a preparation method therefor and an application thereof. Specifically, disclosed is a compound represented by formula I: S-L-E(I), wherein L is a linker chain, which connects S and E by means of covalent bonds; E is the small molecule ligand of an E3 ubiquitin ligase complex. The compound represented by formula I is capable of degrading and/or inhibiting an SOS1 protein in cells, and can be used to treat and/or prevent related diseases or disorders mediated by SOS1, or caused by an interaction between SOS1 and Ras or between SOS1 and Rac.

Description

SOS1降解剂及其制备方法和应用SOS1 degrading agent and preparation method and application thereof 技术领域technical field
本发明属于医药技术领域，具体的，本发明涉及SOS1降解剂，及其制备方法和其作为预防和/或治疗癌症治疗剂的应用。The present invention belongs to the technical field of medicine, and specifically, the present invention relates to a SOS1 degrading agent, a preparation method thereof, and its application as a therapeutic agent for preventing and/or treating cancer.
背景技术Background technique
SOS1(son of sevenless homolog 1)蛋白是一种在细胞中广泛表达的调控蛋白，作为信号通路中的关键蛋白，SOS1在细胞内许多信号转导通路中起着重要的调控作用，例如参与调控Ras和Rac信号通路。SOS1由1333个氨基酸组成，在其C端包含一个富含脯氨酸的结构域(PxxP),该结构域可与Ras通路中的生长因子受体结合蛋白2(growth factor receptor-bound protein 2,Grb2)相结合，形成Grb2和SOS1的复合物，从而将SOS1带至细胞膜Ras蛋白附近，SOS1催化Ras与GTP的结合，促进Ras的激活，进而激活多条下游信号通路，例如Ras-Raf-Mek-Erk、Ras-PI3K-AKT-mTOR。PxxP也可与Rac通路中的E3B1等蛋白的SH3(Src homology 3)结构域相结合，形成EPS8-E3B1-SOS1复合物，EPS8-E3B1-SOS1复合物通过EPS8连接肌动蛋白丝，引起GTP的转换，从而激活Rac，随后激活JNK和MAPK等信号通路。SOS1 (son of sevenless homolog 1) protein is a regulatory protein that is widely expressed in cells. As a key protein in signaling pathways, SOS1 plays an important regulatory role in many signal transduction pathways in cells, such as the regulation of Ras and Rac signaling pathway. SOS1 consists of 1333 amino acids and contains a proline-rich domain (PxxP) at its C-terminus, which can interact with growth factor receptor-bound protein 2 (growth factor receptor-bound protein 2) in the Ras pathway. Grb2) combined to form a complex of Grb2 and SOS1, thereby bringing SOS1 to the vicinity of Ras protein in the cell membrane. SOS1 catalyzes the combination of Ras and GTP, promotes the activation of Ras, and then activates multiple downstream signaling pathways, such as Ras-Raf-Mek -Erk, Ras-PI3K-AKT-mTOR. PxxP can also bind to the SH3 (Src homology 3) domain of proteins such as E3B1 in the Rac pathway to form EPS8-E3B1-SOS1 complexes, which connect actin filaments through EPS8, causing GTP switch, thereby activating Rac, which subsequently activates signaling pathways such as JNK and MAPK.
Ras突变基因被认为是人类癌症具有高发生率的主要致癌基因，研究表明，20-30％的肿瘤患者都存在着Ras的突变，其中KRas的突变占了85％，NRas和HRas分别占12％和3％。然而由于GTP对其结合位点的皮摩尔亲和力，以及Ras蛋白表面光滑，缺乏其他合适的结合口袋，因此，直接作用于Ras抑制其活性被认为是极具挑战性的。Ras mutation gene is considered to be the main oncogene with high incidence of human cancer. Studies have shown that Ras mutation exists in 20-30% of tumor patients, among which KRas mutation accounts for 85%, NRas and HRas account for 12% respectively and 3%. However, directly acting on Ras to inhibit its activity is considered extremely challenging due to the picomolar affinity of GTP for its binding site and the smooth surface of Ras protein and lack of other suitable binding pockets.
SOS1的异常表达或突变与临床疾病的发生也有着密切的关系。研究表明，在NS患者、CFC患者体内都存在SOS1的突变，HGF1是一种罕见的常染色体显性遗传病，其病因也与SOS1的PxxP结构域突变有关，此外，SOS1的异常表达或突变与癌症的发生也有关系。The abnormal expression or mutation of SOS1 is also closely related to the occurrence of clinical diseases. Studies have shown that SOS1 mutations exist in NS patients and CFC patients. HGF1 is a rare autosomal dominant genetic disease, and its etiology is also related to the mutation of the PxxP domain of SOS1. In addition, abnormal expression or mutation of SOS1 is associated with The occurrence of cancer is also related.
WO2018172250A1、WO2020173935A1、WO2019201848A1、WO2020180768A1、WO2020180770A1、WO2019122129A1和EP3558979A1公开了几类SOS1抑制剂，但目前为止，未有SOS1降解剂的相关报道。蛋白降解靶向嵌合体(Proteolysis Targeting Chimeria，PROTAC)是一种不同于传统小分子抑制剂的技术，传统小分子抑制剂通常需要作用于靶蛋白的活性位点才能抑制其活性，而PROTAC为一种异质双功能分子，其一端为可识别靶蛋白的小分子抑制剂，通过连接链，另一端为可识别E3泛素连接酶的E3泛素连接酶配体，这种双功能分子在体内识别靶蛋白和E3泛素连接酶，将靶蛋白和E3泛素连接酶拉近，形成三元复合物，将靶蛋白泛素化后，在体内通过泛素－蛋白酶体途径将靶蛋白降解。相较于传统小分子抑制剂，一方面PROTAC只需要将靶蛋白与E 3泛素连接酶拉近，使底物降解，这种作用模式使得这种技术可以应用于一些不可成药靶点；另一方面，由于靶蛋白在被降解后，PROTAC分子还可释放出来继续参与下一蛋白的降解过程，因此这种具有催化效果的降解作用，使得较少的PROTAC药物剂量就可以实现高效的降解；再一方面，传统的小分子抑制剂易产生耐药性常常是因为发生了点突变，使得小分子抑制剂失去了对靶点的抑制作用，而PROTAC可以直接将靶蛋白降解，在一定程度上能过避免点突变产生的耐药性。因此，相较于传统小分子抑制剂，运用PROTAC技术进行新药小分子研发具有很高的优势和可行性。WO2018172250A1, WO2020173935A1, WO2019201848A1, WO2020180768A1, WO2020180770A1, WO2019122129A1 and EP3558979A1 disclose several types of SOS1 inhibitors, but so far, there is no relevant report on SOS1 degraders. Protein degradation targeting chimera (Proteolysis Targeting Chimeria, PROTAC) is a technology different from traditional small molecule inhibitors, traditional small molecule inhibitors usually need to act on the active site of the target protein to inhibit its activity, while PROTAC is a A heterogeneous bifunctional molecule, one end of which is a small molecule inhibitor that can recognize the target protein, and the other end is an E3 ubiquitin ligase ligand that can recognize E3 ubiquitin ligase. This bifunctional molecule is in vivo It recognizes the target protein and E3 ubiquitin ligase, and draws the target protein and E3 ubiquitin ligase closer to form a ternary complex. After ubiquitinating the target protein, the target protein is degraded in vivo through the ubiquitin-proteasome pathway. Compared with traditional small molecule inhibitors, PROTAC only needs to bring the target protein closer to E3 ubiquitin ligase to degrade the substrate. This mode of action allows this technology to be applied to some undruggable targets; On the one hand, after the target protein is degraded, PROTAC molecules can also be released to continue to participate in the degradation process of the next protein, so this catalytic degradation effect enables efficient degradation with a smaller dose of PROTAC drugs; On the other hand, traditional small-molecule inhibitors are prone to drug resistance, often because of point mutations, which make the small-molecule inhibitors lose their inhibitory effect on the target, while PROTAC can directly degrade the target protein, to a certain extent. Drug resistance caused by point mutations can be avoided. Therefore, compared with traditional small molecule inhibitors, the use of PROTAC technology for the development of new drug small molecules has high advantages and feasibility.
发明内容SUMMARY OF THE INVENTION
本发明提供了式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐The present invention provides compounds of formula I, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable compounds thereof the salt
S-L-ES-L-E
ⅠⅠ
其中：in:
S为能够抑制SOS1蛋白活性或与SOS1蛋白相结合的小分子化合物；S is a small molecule compound that can inhibit the activity of SOS1 protein or bind to SOS1 protein;
L为连接链，其通过共价键连接S和E；L is the linking chain, which connects S and E by covalent bonds;
E为E3泛素连接酶复合体的小分子配体。E is the small molecule ligand of the E3 ubiquitin ligase complex.
本发明提供了式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂 化物、前药和/或其药学上可接受的盐The present invention provides compounds of formula I, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable compounds thereof the salt
S-L-ES-L-E
ⅠⅠ
S、L和E如下文所定义。S, L and E are as defined below.
优选的，本发明某些实施方式中，所述S为S1：Preferably, in some embodiments of the present invention, the S is S1:
Figure PCTCN2022088560-appb-000001
Figure PCTCN2022088560-appb-000001
其中所述S1中：Where said S1:
R 1选自氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、C 1-C 6卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、C 3-C 8环烷基或-C 4-C 8环烯基； R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8 cycloalkenyl;
R 1为-NS(O)(R d)(R e)，所述R d和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、6-10元芳基或5-10元杂芳基； R 1 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 6-10 membered aryl or 5-10 membered heteroaryl;
R 1为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b，所述R a和R b各自独立的为氢、-C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1为-NH-(CH 2) k-NH-C(O)-R aa，所述R aa为C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基(例如所述R aa为C 1-C 6烷基)，且k为1或者2； R 1 is -NH-(CH 2 ) k -NH-C(O)-R aa , wherein R aa is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl (eg, said R aa is C 1 -C 6 alkyl), and k is 1 or 2;
R 1为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b The group is substituted; the R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
或者R 1为 or R 1 as
Figure PCTCN2022088560-appb-000002
Figure PCTCN2022088560-appb-000003
Figure PCTCN2022088560-appb-000004
或者
Figure PCTCN2022088560-appb-000005
Figure PCTCN2022088560-appb-000002
Figure PCTCN2022088560-appb-000003
Figure PCTCN2022088560-appb-000004
or
Figure PCTCN2022088560-appb-000005
或者相邻2个R 1与它们各自连接的碳原子一起形成5-7元环烷基或5-7元杂环烷基； Or adjacent 2 R 1 together with the carbon atoms to which they are attached to form a 5-7 membered cycloalkyl or 5-7 membered heterocycloalkyl;
且所述x为1、2或者3；and said x is 1, 2 or 3;
A 1为C 4-C 12环烷基、杂环烷基、芳基(例如苯基)或杂芳基(例如噻吩基)； A 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl (eg phenyl) or heteroaryl (eg thienyl);
R 2为氢、-OH、氧代、卤素、-CN、C 1-C 6烷基、C 1-C 6烷氧基、C 2-C 6烯基、-C 2-C 6炔基、-C 3-C 8环烷基、-C 3-C 8环烷氧基、-C 3-C 8卤代环烷氧基、-C 4-C 8环烯基、4-7元杂环烷基、-O-CH 2-4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、-C 1-C 6卤代烷基、-C 1-C 6卤代烷氧基、-C 1-C 6烷基磺酰基； R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6 alkylsulfonyl;
R 2为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基或-C(O)C 1-C 3烷基； R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl or -C(O)C 1 -C 3 alkyl;
R 2为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -C(O)NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
R 2为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
R 2为-OR h；所述R h为C 1-C 6烷基； R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
R 2为-(CH 2)NR aR b，所述R a和R b各自独立的氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkane base;
且w为1、2、3或者4(例如，所述w为1、2或3)；and w is 1, 2, 3, or 4 (eg, the w is 1, 2, or 3);
所述A 2(R 3) Y为氢； The A 2 (R 3 ) Y is hydrogen;
或者A 2为C 4-C 12环烷基、杂环烷基、芳基(例如苯基)或杂芳基，且 or A 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl (eg phenyl) or heteroaryl, and
R 3为氢、卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、C 7-C 8环炔基、4-7元杂环烷基、5-10元杂环烯基、苯基、杂芳基、C 1-C 6卤代烷基； R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 7 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-C 1-C 6烷基、-C 1-C 6烷氧基、-C 1-C 6卤代烷基、苯基、杂芳基或-C(O)NR iR j的取代基取代，所述R i和R j各自独立的为氢或者C 1-C 6烷基； The alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR kR l取代，所述R k和R l各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 1-C 6烷基磺酰基、苯基、杂芳基、-CH 2-C(O)-R m、-C(O)R p或4-7元杂环烷基，且所述烷基、炔基、烯基、环烷基、苯基、杂芳基和杂环烷基各自独立的任选的被1个、2个或3个选自C 1-C 6卤代烷基、-OH、氧代基、苯基、-CN、C 1-C 6烷氧基或杂芳基取代，且所述杂芳基任选被甲基取代；且所述R m为双环杂芳基、C 1-C 6烷氧基或者-NR nR o，所述R n和R o各自独立的为氢、C 1-C 6烷基或者苯基，所述烷基任选被C 1-C 6烷氧基或者苯基取代，或者-NR nR o为4-7元氮杂环烷基，所述氮杂环烷基通过N原子连接分子其他部位，且还包含1个或者多个选自N或者O的杂原子；所述R p选自C 1-C 6烷氧基、任选被1个、2个或者3个选自-OH或者C 1-C 6烷氧基取代的C 1-C 6烷基、单环或双环杂芳基、4-7元杂环烷基或者R p为-CH 2-NR qR r，所述R q和R r各自独立的选自氢、苯基或者任选被F取代的C 1-C 6烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl , the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1 - C6 haloalkyl, -OH, oxo base, phenyl, -CN, C 1 -C 6 alkoxy or heteroaryl substituted, and the heteroaryl is optionally substituted with methyl; and the R m is bicyclic heteroaryl, C 1 -C 6 alkoxy or -NR n R o , said R n and R o are each independently hydrogen, C 1 -C 6 alkyl or phenyl, said alkyl optionally being C 1 -C 6 alkoxy Or phenyl substituted, or -NR n R o is a 4-7 membered azacycloalkyl, the azacycloalkyl is connected to other parts of the molecule through an N atom, and also contains 1 or more selected from N or O The heteroatom; the R p is selected from C 1 -C 6 alkoxy, C 1 -C 6 optionally substituted by 1 , 2 or 3 selected from -OH or C 1 -C 6 alkoxy Alkyl, monocyclic or bicyclic heteroaryl, 4-7 membered heterocycloalkyl or R p is -CH 2 -NR q R r , said R q and R r are each independently selected from hydrogen, phenyl or any Select C 1 -C 6 alkyl substituted by F;
或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR sR t取代，所述-NR sR t为通过氮原子连接至分子其他部位的4-7元氮杂环烷基或者通过氮原子连接至分子其他部位的6-10元氮螺杂环烷基，且进一步包括最多两个选自N或者O的杂原子，且任选的被1个、2个或者3个选自-OH、氧代基、C 1-C 6烷基、C 1-C 6羟基烷基、-C(O)OR z的取代基取代，所述R z为C 1-C 6烷基、卤素、-N(C 1-C 6烷基) 2、-CH 2N(C 1-C 6烷基) 2、-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt , the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 alkyl) 2 , -CH 2 N(C 1 - C 6 alkyl) 2 , -C(O)NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
或者R 3为C(O)R v、-C(O)NH 2、-C(O)NHR v、-C(O)NR vR w、-C(O)OR v，所述R v和R w各自独立的为氢、C 1-C 4烷基、C 1-C 4卤代烷基、苯基或者-(CH 2) 2NR xR y，所述R x和R y各自独立的为氢、C 1-C 4烷基或者- (CH 2) 2N(CH 3) 2； or R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 N(CH 3 ) 2 ;
或者R 3为-NH 2、-NHR z、-NR zR za、-NHC(O)R z、-NHC(O)O R z、-NHS(O) 2R z、4-7元杂环烷基、杂芳基、螺杂环烷基、稠杂环烷基、桥杂环烷基，所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； Or R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)O R z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
或者R 3为C 1-C 6烷氧基、C 1-C 6卤代烷氧基、-O(CH 2) s-C 3-C 8环烷基、-O(CH 2) s-苯基、-O(CH 2) s-杂环烷基、-O(CH 2) s-杂芳基，所述s为0、1、2或者3； Or R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
或者R 3为-S(O) 2R z、-S(O) 2NH 2、-S(O) 2NHR z、-S(O) 2NR zR za,所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； or R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
Y为0、1、2、3、4或5(例如，Y为0、1、2或3)；Y is 0, 1, 2, 3, 4, or 5 (eg, Y is 0, 1, 2, or 3);
L'为键、-(CH 2) k-、-O(CH 2) k-、-(CH 2) k-O-或者-O-(CH 2) k-O-(例如，L'为键、-(CH 2) k-或者-O(CH 2) k-)，所述k为0、1、2或者3，或者L'为-CH＝CH-(CH 2) n-,所述n为0、1或者2； L' is a bond, -(CH 2 ) k -, -O(CH 2 ) k -, -(CH 2 ) k -O- or -O-(CH 2 ) k -O- (for example, L' is a bond , -(CH 2 ) k - or -O(CH 2 ) k -), the k is 0, 1, 2 or 3, or L' is -CH=CH-(CH 2 ) n -, the n is 0, 1 or 2;
R 4、R 5各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代。 R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace.
优选的，本发明某些实施方式中，所述S1中R 4、R 5各自独立的为甲基。 Preferably, in some embodiments of the present invention, each of R 4 and R 5 in the S1 is independently a methyl group.
在一些实施方案中，所述S1各基团的定义中，所述R a和R b在任一处出现时各自独立的为氢或C 1-C 6烷基。 In some embodiments, in the definition of each of the groups of S1, the R a and R b at any one occurrence are each independently hydrogen or C 1 -C 6 alkyl.
在一些实施方案中，所述S1各基团的定义中，所述R d和R e在任一处出现时各自独立的为氢或C 1-C 6烷基。 In some embodiments, in the definition of each of the groups of S1, the Rd and Re at any one occurrence are each independently hydrogen or C1 - C6 alkyl.
本发明某些实施方式中，所述S1中，R 5为C 1-C 6烷基，例如甲基。 In certain embodiments of the present invention, in the S1, R 5 is a C 1 -C 6 alkyl group, such as methyl.
本发明某些实施方式中，所述S1中，R 4为C 1-C 6烷基，例如甲基。 In certain embodiments of the present invention, in the S1, R 4 is a C 1 -C 6 alkyl group, such as methyl.
本发明某些实施方式中，所述S1中，R 1为氢或C 1-C 6烷氧基。 In certain embodiments of the present invention, in the S1, R 1 is hydrogen or C 1 -C 6 alkoxy.
本发明某些实施方式中，所述S1中，A 1为芳基或杂芳基。 In certain embodiments of the present invention, in the S1, A 1 is an aryl group or a heteroaryl group.
本发明某些实施方式中，所述S1中，A 1为芳基，例如苯基。 In certain embodiments of the present invention, in the S1, A 1 is an aryl group, such as a phenyl group.
本发明某些实施方式中，所述S1中，A 1为杂芳基，例如噻吩基。 In certain embodiments of the present invention, in the S1, A 1 is a heteroaryl group, such as a thienyl group.
本发明某些实施方式中，所述S1中，R 2为氢、卤素、C 1-C 6烷基或-C 1-C 6卤代烷基。 In certain embodiments of the present invention, in S1, R 2 is hydrogen, halogen, C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
本发明某些实施方式中，所述S1中，L'为键。In some embodiments of the present invention, in the S1, L' is a bond.
本发明某些实施方式中，所述S1中，A 2(R 3) Y为氢。 In certain embodiments of the present invention, in the S1, A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S1中，A 2为芳基，例如苯基。 In certain embodiments of the present invention, in the S1, A 2 is an aryl group, such as a phenyl group.
本发明某些实施方式中，所述S1中，R 3为氢、卤素或C 1-C 6烷基，所述烷基任选被-NR kR l取代；所述R k和R l各自独立的为氢或C 1-C 6烷基。本发明某些实施方式中，所述S7中，R 3为氢、F、Cl、甲基或乙基，所述甲基和乙基被-NR kR l取代；所述R k为甲基或乙基，R l为氢、甲基或乙基。 In some embodiments of the present invention, in the S1, R 3 is hydrogen, halogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted by -NR k R l ; the R k and R l are each independently hydrogen or C1 - C6 alkyl. In some embodiments of the present invention, in the S7, R 3 is hydrogen, F, Cl, methyl or ethyl, and the methyl and ethyl are substituted by -NR k R 1 ; the R k is methyl or ethyl, R l is hydrogen, methyl or ethyl.
本发明某些实施方式中，所述S1中，R 3为氢、Cl、-CH 2NHCH 3或-CH 2N(CH 3) 2。 In some embodiments of the present invention, in the S1, R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
本发明某些实施方式中，所述S1中，A 1为芳基，L'为键，A 2(R 3) Y为氢。 In some embodiments of the present invention, in the S1, A 1 is an aryl group, L' is a bond, and A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S1中，A 1为杂芳基，L'为键，A 2为芳基，R 3为氢、卤素或C 1-C 6烷基，所述烷基任选被-NR kR l取代；所述R k和R l各自独立的为氢或C 1-C 6烷基。 In certain embodiments of the present invention, in the S1, A 1 is a heteroaryl group, L' is a bond, A 2 is an aryl group, and R 3 is hydrogen, halogen or C 1 -C 6 alkyl group, the alkyl group optionally substituted with -NRkRl ; said Rk and Rl are each independently hydrogen or C1 - C6 alkyl.
本发明某些实施方式中，所述S为S1'：In some embodiments of the present invention, the S is S1':
Figure PCTCN2022088560-appb-000006
Figure PCTCN2022088560-appb-000006
其中，所述S1'中，R 1、R 2、R 3、R 4、R 5、L'、A 1、A 2、w、x和Y的定义如S1中所述。 Wherein, in the S1', the definitions of R 1 , R 2 , R 3 , R 4 , R 5 , L', A 1 , A 2 , w, x and Y are as described in S1.
本发明某些实施方式中，所述S为S1”：In some embodiments of the present invention, the S is S1":
Figure PCTCN2022088560-appb-000007
Figure PCTCN2022088560-appb-000007
其中，所述S1”中，R 1、R 2、R 3、R 4、R 5、L'、A 1、A 2、w和Y的定义如S1中所述。 Wherein, in the S1", the definitions of R 1 , R 2 , R 3 , R 4 , R 5 , L′, A 1 , A 2 , w and Y are as described in S1.
本发明某些实施方式中，所述S1'或S1”中，R 1为氢、C 1-C 6烷基或C 1-C 6烷氧基，所述C 1-C 6烷基和C 1-C 6烷氧基任选的被C 1-C 6烷氧基(例如甲氧基)取代。 In certain embodiments of the present invention, in the S1' or S1", R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
本发明某些实施方式中，所述S1'或S1”中，R 1为氢、甲基、甲氧基或
Figure PCTCN2022088560-appb-000008
In some embodiments of the present invention, in the S1' or S1", R 1 is hydrogen, methyl, methoxy or
Figure PCTCN2022088560-appb-000008
本发明某些实施方式中，所述S1和S1'中，
Figure PCTCN2022088560-appb-000009
片段为
Figure PCTCN2022088560-appb-000010
In some embodiments of the present invention, in the S1 and S1',
Figure PCTCN2022088560-appb-000009
Fragment is
Figure PCTCN2022088560-appb-000010
本发明某些实施方式中，所述S为-X-S1'，S1'的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S1', and the structure of S1' is as described above; X is O, NH or S, preferably O.
本发明某些实施方式中，所述S为-X-S1”，S1”的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S1", and the structure of S1" is as described above; X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S1aPreferably, in some embodiments of the present invention, the S is S1a
Figure PCTCN2022088560-appb-000011
Figure PCTCN2022088560-appb-000011
其中所述S1a中：where the S1a:
R 1选自氢、-OCH 3、-OCH 2CH 3、
Figure PCTCN2022088560-appb-000012
-CH 2OH、-C(O)OH、-C(O)OCH 3、-Br、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2、-O(CH 2) 3CH 3、-O(CH 2) 2OCH 3、
Figure PCTCN2022088560-appb-000013
-O(CH 2)-苯基、-N＝S(O)(CH 3) 2、-CH 3、环丙基、-N(CH 3) 2、-NHCH 3、-NH 2、
Figure PCTCN2022088560-appb-000014
Figure PCTCN2022088560-appb-000015
-C(CH 3) 2-OH、
Figure PCTCN2022088560-appb-000016
-NH(CH 2)-NH-C(O)CH 3、-NH(CH 2)-吗啡啉、-NH-C(O)CH 3、-NH-C(O)NHCH 3、-NH-C(O)-N(CH 3) 2、硝基、-NH-S(O) 2CH 3、-N＝S(O)(CH 3) 2、羟基、-O-(CH 2) 2-S(O) 2CH 3、-F、
Figure PCTCN2022088560-appb-000017
Figure PCTCN2022088560-appb-000018
Figure PCTCN2022088560-appb-000019
环丙氧基、环丁氧基、环戊氧基、环己氧基、氮杂环丁烷基、氮杂环戊烷基、哌啶基、哌嗪基、氧杂环丁烷、氧杂环戊烷基、氧杂环己烷基、硫杂环丁烷基、硫杂环戊烷基、硫杂环己烷基、氮杂环丁烷氧基、氮杂环戊烷氧基、哌啶基氧基、哌嗪基氧基、氧杂环丁烷氧基、氧杂环戊烷氧基、氧杂环己烷氧基、硫杂环丁烷氧基、硫杂环戊烷氧基、硫杂环己烷氧基、 R 1 is selected from hydrogen, -OCH 3 , -OCH 2 CH 3 ,
Figure PCTCN2022088560-appb-000012
-CH 2 OH, -C(O)OH, -C(O)OCH 3 , -Br, -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 , -O(CH 2 ) 3 CH 3 , -O(CH 2 ) 2 OCH 3 ,
Figure PCTCN2022088560-appb-000013
-O(CH 2 )-phenyl, -N=S(O)(CH 3 ) 2 , -CH 3 , cyclopropyl, -N(CH 3 ) 2 , -NHCH 3 , -NH 2 ,
Figure PCTCN2022088560-appb-000014
Figure PCTCN2022088560-appb-000015
-C(CH 3 ) 2 -OH,
Figure PCTCN2022088560-appb-000016
-NH(CH 2 )-NH-C(O)CH 3 , -NH(CH 2 )-morpholine, -NH-C(O)CH 3 , -NH-C(O)NHCH 3 , -NH-C (O)-N(CH 3 ) 2 , nitro, -NH-S(O) 2 CH 3 , -N=S(O)(CH 3 ) 2 , hydroxyl, -O-(CH 2 ) 2 -S (O) 2 CH 3 , -F,
Figure PCTCN2022088560-appb-000017
Figure PCTCN2022088560-appb-000018
Figure PCTCN2022088560-appb-000019
Cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy, azetidinyl, azetidinyl, piperidinyl, piperazinyl, oxetane, oxa Cyclopentyl, oxanyl, thietanyl, thietanyl, thietanyl, azetidinyloxy, azepanyloxy, piperidine Peridyloxy, piperazinyloxy, oxetanyloxy, oxolaneoxy, oxaneoxy, thietanyloxy, thietanyloxy , thianeoxy,
Figure PCTCN2022088560-appb-000020
Figure PCTCN2022088560-appb-000021
-OCH 2CH 2CH 3、-OCH 2CH 2CH 2N(CH 3) 2、-OCH 2CH 2CH 2OH、
Figure PCTCN2022088560-appb-000022
Figure PCTCN2022088560-appb-000023
-OCH 2CH 2NC(O)CH 3、-OCH 2CH 2N(CH 3) 2、-OCH 2CH 2OH、
Figure PCTCN2022088560-appb-000024
Figure PCTCN2022088560-appb-000025
-SCH 3、-N(CH 3) 2、
Figure PCTCN2022088560-appb-000026
Figure PCTCN2022088560-appb-000020
Figure PCTCN2022088560-appb-000021
-OCH 2 CH 2 CH 3 , -OCH 2 CH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 CH 2 OH,
Figure PCTCN2022088560-appb-000022
Figure PCTCN2022088560-appb-000023
-OCH 2 CH 2 NC(O)CH 3 , -OCH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 OH,
Figure PCTCN2022088560-appb-000024
Figure PCTCN2022088560-appb-000025
-SCH 3 , -N(CH 3 ) 2 ,
Figure PCTCN2022088560-appb-000026
x为1或者2；x is 1 or 2;
A 1选自
Figure PCTCN2022088560-appb-000027
Figure PCTCN2022088560-appb-000028
A 1 is selected from
Figure PCTCN2022088560-appb-000027
Figure PCTCN2022088560-appb-000028
R 2选自：氢、羟基、氧代基、氰基、环丙基、1，1-二甲基环丙基、-C(＝CH 2)CH 3、-C(CH 3)(＝CH 2)CH 3、-CH＝CH(CH 2) 2CH 3、-CH＝CHCH 3、-CH＝CH-环丙基、-C(O)NH 2、-C(O)OCH 3、-S(O) 2CH 3、-OCH 3、-CH 2NH 2、三氟甲基、甲基、三氟甲氧基、或卤素(F、Cl、Br)、-NH 2、-NHC(O)CH 3、-NHCH 2CH 3或-NHCH(CH 3) 2； R 2 is selected from: hydrogen, hydroxyl, oxo, cyano, cyclopropyl, 1,1-dimethylcyclopropyl, -C(=CH 2 )CH 3 , -C(CH 3 )(=CH 2 ) CH 3 , -CH=CH(CH 2 ) 2 CH 3 , -CH=CHCH 3 , -CH=CH-cyclopropyl, -C(O)NH 2 , -C(O)OCH 3 , -S (O) 2 CH 3 , -OCH 3 , -CH 2 NH 2 , trifluoromethyl, methyl, trifluoromethoxy, or halogen (F, Cl, Br), -NH 2 , -NHC(O) CH 3 , -NHCH 2 CH 3 or -NHCH(CH 3 ) 2 ;
w为1、2或者3；w is 1, 2 or 3;
A 2选自
Figure PCTCN2022088560-appb-000029
Figure PCTCN2022088560-appb-000030
A 2 selected from
Figure PCTCN2022088560-appb-000029
Figure PCTCN2022088560-appb-000030
R 3选自-C(O)NH(CH 2) 2CH 3、-C(O)N(CH 3) 2、-C(O)NH 2、-C(O)NH(CH 2) 2N(CH 3) 2、-CH 2C(O)NH 2、氢、-F、-Cl、-Br、氰基、-CF 3、-CH 3、-CH 2CH 3、-CH＝CH 2、-CH 2CN、-CH(CH 3)-NH 2、-CH＝CH-CN、-C(O)-OH、-C(O)OCH 3、-C(O)CH 3、-C(CH 3) 2-C(O)-OCH 3、-C(CH 3) 2-CN、氧代基、羟基、环丙基、环丁基、环戊基、-NH 2、-NH-C(O)CH 3、-NH-S(O) 2CH 3、-NH-C(O)OC(CH 3) 3、
Figure PCTCN2022088560-appb-000031
Figure PCTCN2022088560-appb-000032
-S(O) 2CH 3、-S(O) 2NCH 3、-S(O) 2NH 2、-OCH 2CH 3、-O(CH 2) 2CH 3、-OCF 3、
Figure PCTCN2022088560-appb-000033
-OCH 2环丙基、-OCH 3、-O(CH 2) 3CH 3、-OCH 2苯基、-O-苯基、-(CH 2)-OH、-(CH 2) 2-OH、-(CH 2)-OCH 3、-(CH 2)-OCH 2CH 3、-CH(OH)-CH 2-苯基、-CH(OH)-CH 2CH 3、-CH(OH)-CH 2CH 2CH 3、-CH(OH)-CH 2CH 2CH 2CH 3、-CH(OH)-CH(CH 3) 2、-CH(OH)-苯基、-CH(OH)-CN、-CH(OH)-CH 2-OH、-CH(OH)-CF 3、-CH(OH)-(CH 2) 2-苯基、 ＊-CH(OH)-C≡CH、-CH(NH 2)-CH 2-C(O)OH、-CH 2-NH-S(O) 2-CH 3、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2、-CH 2-NH-CH 2CH 3、-CH(CH 3)-NH 2、-CH 2-NH 2、-CH 2CH 2-NH 2、-CH 2NH-CH 2-苯基、-CH 2N(CH 2CH 3) 2、-CH 2NH-环丙基、-CH 2NH-环丁基、-CH 2NH-环戊基、-CH 2NH-吡啶基、-CH 2NH-苯基、-CH 2NH-(CH 2) 2-OH、-CH 2N(CH 3)-(CH 2) 2-OH、-CH 2NH-CH 2-CN、-CH 2N(CH 3)-CH 2-CN、-CH 2N(CH 3)-CH 2-CF 3、-CH 2N(CH 3)-CH 2-CF 2H、-CH 2NH-CH 2-CF 2H、-CH 2NH-(CH 2) 2-OCH 3、
Figure PCTCN2022088560-appb-000034
Figure PCTCN2022088560-appb-000035
Figure PCTCN2022088560-appb-000036
-CH 2NH-C(O)-OC(CH 3) 3、-CH 2CH 2NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 2NOH、-CH 2NH-C(O)-CH 2OCH 3、-CH(CH 3)NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 3、
Figure PCTCN2022088560-appb-000037
-CH 2NHCH 2-C(O)-NH 2、-CH 2NHCH 2-C(O)-(CH 3) 2、-CH 2NHCH 2-C(O)-OCH 3、-CH 2NHCH 2-C(O)-NHCH 3、-CH 2NHCH 2-C(O)-NH(CH 2) 2-OCH 3、-CH 2NHCH 2-C(O)-NHCH 2-苯基、
Figure PCTCN2022088560-appb-000038
-CH 2NHCH 2-C(O)-NH-苯基、
Figure PCTCN2022088560-appb-000039
-CH 2NH- C(O)-CH 2NH-苯基、
Figure PCTCN2022088560-appb-000040
Figure PCTCN2022088560-appb-000041
或-CH 2NH-C(O)-CH 2NH-CH 2CF 3； R3 is selected from -C(O)NH( CH2 ) 2CH3 , -C(O)N( CH3 ) 2 , -C(O) NH2 , -C (O)NH( CH2 ) 2N (CH 3 ) 2 , -CH 2 C(O)NH 2 , hydrogen, -F, -Cl, -Br, cyano, -CF 3 , -CH 3 , -CH 2 CH 3 , -CH=CH 2 , -CH 2 CN, -CH(CH 3 )-NH 2 , -CH=CH-CN, -C(O)-OH, -C(O)OCH 3 , -C(O)CH 3 , -C(CH 3 ) 2 -C(O)-OCH 3 , -C(CH 3 ) 2 -CN, oxo, hydroxyl, cyclopropyl, cyclobutyl, cyclopentyl, -NH 2 , -NH-C(O )CH 3 , -NH-S(O) 2 CH 3 , -NH-C(O)OC(CH 3 ) 3 ,
Figure PCTCN2022088560-appb-000031
Figure PCTCN2022088560-appb-000032
-S(O) 2 CH 3 , -S(O) 2 NCH 3 , -S(O) 2 NH 2 , -OCH 2 CH 3 , -O(CH 2 ) 2 CH 3 , -OCF 3 ,
Figure PCTCN2022088560-appb-000033
-OCH 2 cyclopropyl, -OCH 3 , -O(CH 2 ) 3 CH 3 , -OCH 2 phenyl, -O-phenyl, -(CH 2 )-OH, -(CH 2 ) 2 -OH, -(CH 2 )-OCH 3 , -(CH 2 )-OCH 2 CH 3 , -CH(OH)-CH 2 -phenyl, -CH(OH)-CH 2 CH 3 , -CH(OH)-CH 2CH2CH3 , -CH(OH ) -CH2CH2CH2CH3 , -CH(OH ) -CH ( CH3 ) 2 , -CH(OH ) -phenyl, -CH(OH)-CN , -CH(OH)-CH 2 -OH, -CH(OH)-CF 3 , -CH(OH)-(CH 2 ) 2 -phenyl, * -CH(OH)-C≡CH, -CH( NH 2 )-CH 2 -C(O)OH, -CH 2 -NH-S(O) 2 -CH 3 , -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 , -CH 2 -NH-CH 2 CH 3 , -CH(CH 3 )-NH 2 , -CH 2 -NH 2 , -CH 2 CH 2 -NH 2 , - CH2NH - CH2 -phenyl, -CH2N(CH2CH3)2 , -CH2NH - cyclopropyl , -CH2NH - cyclobutyl, -CH2NH - cyclopentyl, - CH2NH -pyridyl, -CH2NH-phenyl, -CH2NH-( CH2 ) 2 -OH, -CH2N ( CH3 )-( CH2 ) 2 - OH, -CH2NH- CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CF 3 , -CH 2 N(CH 3 )-CH 2 -CF 2 H, -CH 2 NH-CH 2 -CF 2 H, -CH 2 NH-(CH 2 ) 2 -OCH 3 ,
Figure PCTCN2022088560-appb-000034
Figure PCTCN2022088560-appb-000035
Figure PCTCN2022088560-appb-000036
-CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 2 NOH, -CH 2 NH-C(O)-CH 2 OCH 3 , -CH(CH 3 )NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 3 ,
Figure PCTCN2022088560-appb-000037
-CH 2 NHCH 2 -C(O)-NH 2 , -CH 2 NHCH 2 -C(O)-(CH 3 ) 2 , -CH 2 NHCH 2 -C(O)-OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 3 , -CH 2 NHCH 2 -C(O)-NH(CH 2 ) 2 -OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 2 -phenyl,
Figure PCTCN2022088560-appb-000038
-CH 2 NHCH 2 -C(O)-NH-phenyl,
Figure PCTCN2022088560-appb-000039
-CH 2 NH- C(O)-CH 2 NH-phenyl,
Figure PCTCN2022088560-appb-000040
Figure PCTCN2022088560-appb-000041
or -CH 2 NH-C(O)-CH 2 NH-CH 2 CF 3 ;
Y为1或者2；Y is 1 or 2;
L'为键、-(CH 2) k-或者-O(CH 2) k-，所述k为1或者2，或者L'为-CH＝CH-(CH 2) n-，所述n为0、1或者2。 L' is a bond, -(CH 2 ) k - or -O(CH 2 ) k -, the k is 1 or 2, or L' is -CH=CH-(CH 2 ) n -, the n is 0, 1 or 2.
在一些实施方案中，所述S1a中，R 2选自：氢、羟基、氧代基、氰基、环丙基、1，1-二甲基环丙基、-C(＝CH 2)CH 3、-C(CH 3)(＝CH 2)CH 3、-CH＝CH(CH 2) 2CH 3、-CH＝CHCH 3、-CH＝CH-环丙基、-C(O)NH 2、-C(O)OCH 3、-S(O) 2CH 3、-OCH 3、-CH 2NH 2、三氟甲基、甲基、三氟甲氧基、卤素(F、Cl、Br)。 In some embodiments, in the S1a, R 2 is selected from the group consisting of: hydrogen, hydroxyl, oxo, cyano, cyclopropyl, 1,1-dimethylcyclopropyl, -C(=CH 2 )CH 3 , -C(CH 3 )(=CH 2 )CH 3 , -CH=CH(CH 2 ) 2 CH 3 , -CH=CHCH 3 , -CH=CH-cyclopropyl, -C(O)NH 2 , -C(O)OCH 3 , -S(O) 2 CH 3 , -OCH 3 , -CH 2 NH 2 , trifluoromethyl, methyl, trifluoromethoxy, halogen (F, Cl, Br) .
本发明某些实施方式中，所述S1a中，w为1或者2。In some embodiments of the present invention, in the S1a, w is 1 or 2.
本发明某些实施方式中，所述S1a中，R 1为氢、-CH 3、-OCH 3、-OCH 2CH 3、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2或-O(CH 2) 3CH 3，例如-OCH 3。 In some embodiments of the present invention, in the S1a, R 1 is hydrogen, -CH 3 , -OCH 3 , -OCH 2 CH 3 , -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 or -O( CH2 ) 3CH3 , eg -OCH3 .
本发明某些实施方式中，所述S1a中，A 1为
Figure PCTCN2022088560-appb-000042
In some embodiments of the present invention, in the S1a, A 1 is
Figure PCTCN2022088560-appb-000042
本发明某些实施方式中，所述S1a中，A 1为
Figure PCTCN2022088560-appb-000043
In some embodiments of the present invention, in the S1a, A 1 is
Figure PCTCN2022088560-appb-000043
本发明某些实施方式中，所述S1a中，R 2为氢、卤素、-NH 2、C 1-C 6烷基或-C 1-C 6卤代烷基。 In certain embodiments of the present invention, in the S1a, R 2 is hydrogen, halogen, -NH 2 , C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
本发明某些实施方式中，所述S1a中，L'为键。In some embodiments of the present invention, in the S1a, L' is a bond.
本发明某些实施方式中，所述S1a中，A 2(R 3) Y为氢。 In certain embodiments of the present invention, in the S1a, A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S1a中，A 2为
Figure PCTCN2022088560-appb-000044
In some embodiments of the present invention, in the S1a, A 2 is
Figure PCTCN2022088560-appb-000044
本发明某些实施方式中，所述S1a中，R 3为氢、-F、-Cl、-Br、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2或-CH 2-NH-CH 2CH 3。 In some embodiments of the present invention, in the S1a, R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH2 -N( CH3 ) 2 or -CH2 -NH - CH2CH3 .
本发明某些实施方式中，所述S1a中，R 3为氢、Cl、-CH 2NHCH 3或-CH 2N(CH 3) 2。 In certain embodiments of the present invention, in the S1a, R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
本发明某些实施方式中，所述S1a中，A 1为
Figure PCTCN2022088560-appb-000045
L'为键，A 2(R 3) Y为氢。 In some embodiments of the present invention, in the S1a, A 1 is
Figure PCTCN2022088560-appb-000045
L' is a bond, and A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S1a中，A 1为
Figure PCTCN2022088560-appb-000046
L'为键，A 2为
Figure PCTCN2022088560-appb-000047
R 3为氢、-F、-Cl、-Br、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2或-CH 2-NH-CH 2CH 3。 In some embodiments of the present invention, in the S1a, A 1 is
Figure PCTCN2022088560-appb-000046
L' is the key, A 2 is
Figure PCTCN2022088560-appb-000047
R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 or -CH 2 -NH - CH2CH3 .
本发明某些实施方式中，所述S为S1a'：In some embodiments of the present invention, the S is S1a':
Figure PCTCN2022088560-appb-000048
Figure PCTCN2022088560-appb-000048
其中，所述S1a'中，R 1、R 2、R 3、L'、A 1、A 2、w、x和Y的定义如S1或S1a中所述。 Wherein, in the S1a', the definitions of R 1 , R 2 , R 3 , L', A 1 , A 2 , w, x and Y are as described in S1 or S1a.
本发明某些实施方式中，所述S为S1a”：In some embodiments of the present invention, the S is S1a":
Figure PCTCN2022088560-appb-000049
Figure PCTCN2022088560-appb-000049
其中，所述S1a”中，R 1、R 2、R 3、L'、A 1、A 2、w和Y的定义如S1或S1a中所述。 Wherein, in said S1a", the definitions of R 1 , R 2 , R 3 , L', A 1 , A 2 , w and Y are as described in S1 or S1a.
本发明某些实施方式中，所述S1a'、S1a”中，R 1为氢、C 1-C 6烷基或C 1-C 6烷氧基，所述C 1-C 6烷基和C 1-C 6烷氧基任选的被C 1-C 6烷氧基(例如甲氧基)取代。 In certain embodiments of the present invention, in the S1a', S1a", R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
本发明某些实施方式中，所述S1a'、S1a”中，R 1为氢、甲基、甲氧基或
Figure PCTCN2022088560-appb-000050
In some embodiments of the present invention, in the S1a', S1a", R 1 is hydrogen, methyl, methoxy or
Figure PCTCN2022088560-appb-000050
本发明某些实施方式中，所述S1a、S1a'、S1a”中，
Figure PCTCN2022088560-appb-000051
片段为
Figure PCTCN2022088560-appb-000052
In some embodiments of the present invention, in the S1a, S1a', S1a",
Figure PCTCN2022088560-appb-000051
Fragment is
Figure PCTCN2022088560-appb-000052
本发明某些实施方式中，所述S为-X-S1a'，S1a'的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S1a', and the structure of S1a' is as described above; X is O, NH or S, preferably O.
本发明某些实施方式中，所述S为-X-S1a”，S1a”的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S1a", and the structure of S1a" is as described above; X is O, NH or S, preferably O.
更优选的，本发明某些实施方式中，所述S1为WO2018172250A1(其全文通过引用的方式并入本文中)中实施例1(Example 1)至实施例458(Example 458)的具体化合物。More preferably, in certain embodiments of the present invention, the S1 is the specific compound of Example 1 (Example 1) to Example 458 (Example 458) in WO2018172250A1 (which is incorporated herein by reference in its entirety).
优选的，本发明某些实施方式中，所述S为S2：Preferably, in some embodiments of the present invention, the S is S2:
Figure PCTCN2022088560-appb-000053
Figure PCTCN2022088560-appb-000053
其中所述S2中：where the S2:
R 1为氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b；所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkyl mercapto or -NR a R b ; the R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、C 1-C 6卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、C 3-C 8环烷基或-C 4-C 8环烯基； R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8 cycloalkenyl;
R 1为-NS(O)(R d)(R e)，所述R d和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基； R 1 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl;
R 1为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b,所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷 基或C 3-C 8环烷基； R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, C 1 -C 6 alkyl , C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1为-NH-(CH 2) k-NH-C(O)-(C 1-C 6烷基)，所述k为1或者2； R 1 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
R 1为-NH-(CH 2) i-R f，所述i为0、1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b The group is substituted; the R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 1为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
或者R 1为 or R 1 as
Figure PCTCN2022088560-appb-000054
Figure PCTCN2022088560-appb-000055
所述L 2a为C(O),L 2b为键或C 1-C 6亚烷基，X 2为
Figure PCTCN2022088560-appb-000054
Figure PCTCN2022088560-appb-000055
Described L 2 a is C(O), L 2 b is bond or C 1 -C 6 alkylene, X 2 is
Figure PCTCN2022088560-appb-000056
Rx 2为
Figure PCTCN2022088560-appb-000057
Figure PCTCN2022088560-appb-000056
Rx 2 is
Figure PCTCN2022088560-appb-000057
或者R 1为 or R 1 as
Figure PCTCN2022088560-appb-000058
Figure PCTCN2022088560-appb-000059
或者
Figure PCTCN2022088560-appb-000060
Figure PCTCN2022088560-appb-000058
Figure PCTCN2022088560-appb-000059
or
Figure PCTCN2022088560-appb-000060
或者相邻2个R 1与它们各自连接的碳原子一起形成5-7元环烷基或5-7元杂环烷基； Or adjacent 2 R 1 together with the carbon atoms to which they are attached to form a 5-7 membered cycloalkyl or 5-7 membered heterocycloalkyl;
且所述x为1、2、3或者4(例如，所述x为1、2或3)；and said x is 1, 2, 3, or 4 (eg, said x is 1, 2, or 3);
A 1为C 4-C 12环烷基、杂环烷基、芳基或杂芳基； A 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl;
R 2为氢、-OH、氧代、卤素、-CN、C 1-C 6烷基、C 1-C 6烷氧基、C 2-C 6烯基、-C 2-C 6炔基、-C 3-C 8环烷基、-C 3-C 8环烷氧基、-C 3-C 8卤代环烷氧基、-C 4-C 8环烯基、4-7元杂环烷基、-O-CH 2-4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、-C 1-C 6卤代烷基、-C 1-C 6卤代烷氧基、-C 1-C 6烷基磺酰基； R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6 alkylsulfonyl;
R 2为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 2为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
R 2为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
R 2为-OR h；所述R h为C 1-C 6烷基； R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
R 2为-(CH 2)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -(CH 2 )NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl, or C 3 -C 8 ring alkyl;
且w为1、2、3或者4(例如，所述w为1或者2)；and w is 1, 2, 3, or 4 (eg, the w is 1 or 2);
所述A 2(R 3) Y为氢； The A 2 (R 3 ) Y is hydrogen;
或者A 2为C 4-C 12环烷基、杂环烷基、芳基或杂芳基，且 or A 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl, and
R 3为氢、卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、C 2-C 8环炔基、4-7元杂环烷基、5-10元杂环烯基、苯基、杂芳基、C 1-C 6卤代烷基； R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 2 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-C 1-C 6烷基、-C 1-C 6烷氧基、-C 1-C 6卤代烷基、苯基、杂芳基或-C(O)NR iR j的取代基取代，所述R i和R j各自独立的为氢或者C 1-C 6烷基； The alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR kR l取代，所述R k和R l各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 1-C 6烷基磺酰基、苯基、杂芳基、-CH 2-C(O)-R m、-C(O)R p或4-7元杂环烷基，且所述烷基、炔基、烯基、环烷基、苯基、杂芳基和杂环烷基各自独立的任选的被1个、2个或3个选自C 1-C 6卤代烷基、-OH、氧代基、苯基、-CN、C 1-C 6烷氧基或杂芳基取代，且所述杂芳基任选被甲基取代；且所述R m为双环杂芳基、C 1-C 6烷氧基或者-NR nR o，所述R n和R o各自独立的为氢、C 1-C 6烷基或者苯基，所述烷基任选被C 1-C 6烷氧基或者苯基取代，或者-NR nR o为4-7元氮杂环烷基，所述氮杂环烷基通过N原子连接分子其他部位，且还包含1个或者多个选自N或者O的杂原子；所述R p选自C 1-C 6烷氧基、任选被1个、2个或者3个选自-OH或者C 1-C 6烷氧基取代的C 1-C 6烷基、单环或双环杂芳基、4-7元杂环烷基或者R p为-CH 2-NR qR r，所述R q和R r各自独立的选自氢、苯基或者任选被F取代的C 1-C 6烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl , the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1 - C6 haloalkyl, -OH, oxo base, phenyl, -CN, C 1 -C 6 alkoxy or heteroaryl substituted, and the heteroaryl is optionally substituted with methyl; and the R m is bicyclic heteroaryl, C 1 -C 6 alkoxy or -NR n R o , said R n and R o are each independently hydrogen, C 1 -C 6 alkyl or phenyl, said alkyl optionally being C 1 -C 6 alkoxy Or phenyl substituted, or -NR n R o is a 4-7 membered azacycloalkyl, the azacycloalkyl is connected to other parts of the molecule through an N atom, and also contains 1 or more selected from N or O The heteroatom; the R p is selected from C 1 -C 6 alkoxy, C 1 -C 6 optionally substituted by 1 , 2 or 3 selected from -OH or C 1 -C 6 alkoxy Alkyl, monocyclic or bicyclic heteroaryl, 4-7 membered heterocycloalkyl or R p is -CH 2 -NR q R r , said R q and R r are each independently selected from hydrogen, phenyl or any Select C 1 -C 6 alkyl substituted by F;
或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR sR t取代，所述-NR sR t为通过氮原子连接至分子其他部位的4-7元氮杂环烷基或者通过氮原子连接至分子其他部位的6-10元氮螺杂环烷基，且进一步包括最多两个选自N或者O的杂原子，且任选的被1个、2个或者3个选自-OH、氧代基、C 1-C 6烷基、C 1-C 6羟基烷基、-C(O)OR z的取代基取代，所述R z为C 1-C 6烷基、卤素、-N(C 1-C 6烷基) 2、-CH 2N(C 1-C 6烷基) 2、-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt , the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 alkyl) 2 , -CH 2 N(C 1 - C 6 alkyl) 2 , -C(O)NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
或者R 3为C(O)R v、-C(O)NH 2、-C(O)NHR v、-C(O)NR vR w、-C(O)OR v，所述R v和R w各自独立的为氢、C 1-C 4烷基、C 1-C 4卤代烷基、苯基或者-(CH 2) 2NR xR y，所述R x和R y各自独立的为氢、C 1-C 4烷基或者-(CH 2) 2NH(CH 3) 2； or R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 NH(CH 3 ) 2 ;
或者R 3为-NH 2、-NHR z、-NR zR za、-NHC(O)R z、-NHC(O)O R z、-NHS(O) 2R z、4-7元杂环烷基、杂芳基、螺杂环烷基、稠杂环烷基、桥杂环烷基，所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； Or R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)O R z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
或者R 3为C 1-C 6烷氧基、C 1-C 6卤代烷氧基、-O(CH 2) s-C 3-C 8环烷基、-O(CH 2) s-苯基、-O(CH 2) s-杂环烷基、-O(CH 2) s-杂芳基，所述s为0、1、2或者3； Or R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
或者R 3为-S(O) 2R z、-S(O) 2NH 2、-S(O) 2NHR z、-S(O) 2NR zR za,所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； or R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
Y为0、1、2、3、4或5(例如，所述Y为0、1、2或3)；Y is 0, 1, 2, 3, 4, or 5 (eg, the Y is 0, 1, 2, or 3);
L'为键、-(CH 2) k-、-O(CH 2) k-、-(CH 2) k-O-或者-O-(CH 2) k-O-(例如，所述L'为键、-(CH 2) k-或-O(CH 2) k-)，所述k为0、1、2或者3，或者L'为-CH＝CH-(CH 2) n-,所述n为0、1或者2； L' is a bond, -(CH 2 ) k -, -O(CH 2 ) k -, -(CH 2 ) k -O-, or -O-(CH 2 ) k -O- (eg, the L' is a bond, -(CH 2 ) k - or -O(CH 2 ) k -), the k is 0, 1, 2 or 3, or L' is -CH=CH-(CH 2 ) n -, the Said n is 0, 1 or 2;
R 4、R 5各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代； R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace;
T和V都为N，或者T为C，V为N，或者T为N，V为C。Both T and V are N, or T is C and V is N, or T is N and V is C.
优选的，本发明某些实施方式中，所述S2中R 4、R 5各自独立的为甲基。 Preferably, in some embodiments of the present invention, each of R 4 and R 5 in the S2 is independently a methyl group.
在一些实施方案中，所述S2各基团的定义中，所述R a和R b在任一处出现时各自独立的为氢或C 1-C 6烷基。 In some embodiments, in the definition of each group of S2, each of said Ra and Rb at any occurrence is independently hydrogen or C1 - C6 alkyl.
本发明某些实施方式中，所述S2中，T和V都为N。In some embodiments of the present invention, in the S2, both T and V are N.
本发明某些实施方式中，所述S2中，T为C，V为N。In some embodiments of the present invention, in the S2, T is C, and V is N.
本发明某些实施方式中，所述S2中，T为N，V为C。In some embodiments of the present invention, in S2, T is N, and V is C.
本发明某些实施方式中，所述S2中，R 5为C 1-C 6烷基，例如甲基。 In certain embodiments of the present invention, in the S2, R 5 is a C 1 -C 6 alkyl group, such as methyl.
本发明某些实施方式中，所述S2中，R 4为C 1-C 6烷基，例如甲基。 In certain embodiments of the present invention, in the S2, R 4 is a C 1 -C 6 alkyl group, such as methyl.
本发明某些实施方式中，所述S2中，R 1为氢或C 1-C 6烷氧基。 In certain embodiments of the present invention, in the S2, R 1 is hydrogen or C 1 -C 6 alkoxy.
本发明某些实施方式中，所述S2中，A 1为芳基或杂芳基。 In certain embodiments of the present invention, in the S2, A 1 is an aryl group or a heteroaryl group.
本发明某些实施方式中，所述S2中，A 1为芳基，例如苯基。 In certain embodiments of the present invention, in the S2, A 1 is an aryl group, such as a phenyl group.
本发明某些实施方式中，所述S2中，A 1为杂芳基，例如噻吩基。 In certain embodiments of the present invention, in the S2, A 1 is a heteroaryl group, such as a thienyl group.
本发明某些实施方式中，所述S2中，R 2为氢、卤素、C 1-C 6烷基或-C 1-C 6卤代烷基。 In certain embodiments of the present invention, in the S2, R 2 is hydrogen, halogen, C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
本发明某些实施方式中，所述S2中，L'为键。In some embodiments of the present invention, in the S2, L' is a bond.
本发明某些实施方式中，所述S2中，A 2(R 3) Y为氢。 In some embodiments of the present invention, in the S2, A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S2中，A 2为芳基，例如苯基。 In certain embodiments of the present invention, in the S2, A 2 is an aryl group, such as a phenyl group.
本发明某些实施方式中，所述S2中，R 3为氢、卤素或C 1-C 6烷基，所述烷基任选被-NR kR l取代；所述R k和R l各自独立的为氢或C 1-C 6烷基。本发明某些实施方式中，所述S7中，R 3为氢、F、Cl、甲基或乙基，所述甲基和乙基被-NR kR l取代；所述R k为甲基或乙基，R l为氢、甲基或乙基。 In some embodiments of the present invention, in the S2, R 3 is hydrogen, halogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted by -NR k R l ; the R k and R l are each independently hydrogen or C1 - C6 alkyl. In some embodiments of the present invention, in the S7, R 3 is hydrogen, F, Cl, methyl or ethyl, and the methyl and ethyl are substituted by -NR k R 1 ; the R k is methyl or ethyl, R l is hydrogen, methyl or ethyl.
本发明某些实施方式中，所述S2中，R 3为氢、Cl、-CH 2NHCH 3或-CH 2N(CH 3) 2。 In some embodiments of the present invention, in the S2, R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
本发明某些实施方式中，所述S2中，A 1为芳基，L'为键，A 2(R 3) Y为氢。 In some embodiments of the present invention, in S2, A 1 is an aryl group, L' is a bond, and A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S2中，A 1为杂芳基，L'为键，A 2为芳基，R 3为氢、卤素或C 1-C 6烷基，所述烷基任选被-NR kR l取代；所述R k和R l各自独立的为氢或C 1-C 6烷基。 In some embodiments of the present invention, in the S2, A 1 is a heteroaryl group, L' is a bond, A 2 is an aryl group, R 3 is hydrogen, halogen or C 1 -C 6 alkyl group, the alkyl group optionally substituted with -NRkRl ; said Rk and Rl are each independently hydrogen or C1 - C6 alkyl.
本发明某些实施方式中，所述S为S2'：In some embodiments of the present invention, the S is S2':
Figure PCTCN2022088560-appb-000061
Figure PCTCN2022088560-appb-000061
其中，所述S2'中，T、V、R 1、R 2、R 3、R 4、R 5、L'、A 1、A 2、w、x和Y的定义如S2中所述。 Wherein, in the S2', the definitions of T, V, R 1 , R 2 , R 3 , R 4 , R 5 , L', A 1 , A 2 , w, x and Y are as described in S2.
本发明某些实施方式中，所述S为S2”：In some embodiments of the present invention, the S is S2":
Figure PCTCN2022088560-appb-000062
Figure PCTCN2022088560-appb-000062
其中，所述S2”中，R 2、R 3、R 4、R 5、L'、A 1、A 2、w和Y的定义如S2中所述。 Wherein, in the S2", the definitions of R 2 , R 3 , R 4 , R 5 , L′, A 1 , A 2 , w and Y are as described in S2.
本发明某些实施方式中，所述S2、S2'、S2”中，R 1为氢、C 1-C 6烷基或C 1-C 6烷氧基，所述C 1-C 6烷基和C 1-C 6烷氧基任选的被C 1-C 6烷氧基(例如甲氧基)取代。 In certain embodiments of the present invention, in the S2, S2', S2", R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, and the C 1 -C 6 alkyl and C 1 -C 6 alkoxy optionally substituted with C 1 -C 6 alkoxy (eg, methoxy).
本发明某些实施方式中，所述S2、S2'、S2”中，R 1为氢、甲基、甲氧基或
Figure PCTCN2022088560-appb-000063
In some embodiments of the present invention, in the S2, S2', S2", R 1 is hydrogen, methyl, methoxy or
Figure PCTCN2022088560-appb-000063
本发明某些实施方式中，所述S2和S2'中，
Figure PCTCN2022088560-appb-000064
片段为
Figure PCTCN2022088560-appb-000065
In some embodiments of the present invention, in the S2 and S2',
Figure PCTCN2022088560-appb-000064
Fragment is
Figure PCTCN2022088560-appb-000065
本发明某些实施方式中，所述S为-X-S2'，S2'的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S2', and the structure of S2' is as described above; X is O, NH or S, preferably O.
本发明某些实施方式中，所述S为-X-S2”，S2”的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S2", and the structure of S2" is as described above; X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S2a，Preferably, in some embodiments of the present invention, the S is S2a,
Figure PCTCN2022088560-appb-000066
Figure PCTCN2022088560-appb-000066
其中所述S2a中：Where said S2a:
T和V都为N，或者T为C，V为N，或者T为N，V为C；Both T and V are N, or T is C and V is N, or T is N and V is C;
R 1选自氢、-OCH 3、-OCH 2CH 3、
Figure PCTCN2022088560-appb-000067
-CH 2OH、-C(O)OH、-C(O)OCH 3、-Br、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2、-O(CH 2) 3CH 3、-O(CH 2) 2OCH 3、
Figure PCTCN2022088560-appb-000068
-O(CH 2) z-苯基、-N＝S(O)(CH 3) 2、-CH 3、环丙基、-N(CH 3) 2、-NHCH 3、-NH 2、
Figure PCTCN2022088560-appb-000069
Figure PCTCN2022088560-appb-000070
-C(CH 3) 2-OH、
Figure PCTCN2022088560-appb-000071
-NH(CH 2)-NH-C(O)CH 3、-NH(CH 2)-吗啡啉、-NH-C(O)CH 3、-NH-C(O)NHCH 3、-NH-C(O)-N(CH 3) 2、硝基、-NH-S(O) 2CH 3、-N＝S(O)(CH 3) 2、羟基、-O-(CH 2) 2-S(O) 2CH 3、-F、
Figure PCTCN2022088560-appb-000072
Figure PCTCN2022088560-appb-000073
Figure PCTCN2022088560-appb-000074
环丙氧基、环丁氧基、环戊氧基、环己氧基、氮杂环丁烷基、氮杂环戊烷基、哌啶基、哌嗪基、氧杂环丁烷、氧杂环戊烷基、氧杂环己烷基、硫杂环丁烷基、硫杂环戊烷基、硫杂环己烷基、氮杂环丁烷氧基、氮杂环戊烷氧基、哌啶基氧基、哌嗪基氧基、氧杂环丁烷氧基、氧杂环戊烷氧基、氧杂环己烷氧基、硫杂环丁烷氧基、硫杂环戊烷氧基、硫杂环己烷氧基、 R 1 is selected from hydrogen, -OCH 3 , -OCH 2 CH 3 ,
Figure PCTCN2022088560-appb-000067
-CH 2 OH, -C(O)OH, -C(O)OCH 3 , -Br, -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 , -O(CH 2 ) 3 CH 3 , -O(CH 2 ) 2 OCH 3 ,
Figure PCTCN2022088560-appb-000068
-O(CH 2 ) z -phenyl, -N=S(O)(CH 3 ) 2 , -CH 3 , cyclopropyl, -N(CH 3 ) 2 , -NHCH 3 , -NH 2 ,
Figure PCTCN2022088560-appb-000069
Figure PCTCN2022088560-appb-000070
-C(CH 3 ) 2 -OH,
Figure PCTCN2022088560-appb-000071
-NH(CH 2 )-NH-C(O)CH 3 , -NH(CH 2 )-morpholine, -NH-C(O)CH 3 , -NH-C(O)NHCH 3 , -NH-C (O)-N(CH 3 ) 2 , nitro, -NH-S(O) 2 CH 3 , -N=S(O)(CH 3 ) 2 , hydroxyl, -O-(CH 2 ) 2 -S (O) 2 CH 3 , -F,
Figure PCTCN2022088560-appb-000072
Figure PCTCN2022088560-appb-000073
Figure PCTCN2022088560-appb-000074
Cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy, azetidinyl, azetidinyl, piperidinyl, piperazinyl, oxetane, oxa Cyclopentyl, oxanyl, thietanyl, thietanyl, thietanyl, azetidinyloxy, azepanyloxy, piperidine Peridyloxy, piperazinyloxy, oxetanyloxy, oxolaneoxy, oxaneoxy, thietanyloxy, thietanyloxy , thianeoxy,
Figure PCTCN2022088560-appb-000075
Figure PCTCN2022088560-appb-000076
-OCH 2CH 2CH 3、-OCH 2CH 2CH 2N(CH 3) 2、-OCH 2CH 2CH 2OH、
Figure PCTCN2022088560-appb-000077
Figure PCTCN2022088560-appb-000078
-OCH 2CH 2NC(O)CH 3、-OCH 2CH 2N(CH 3) 2、-OCH 2CH 2OH、
Figure PCTCN2022088560-appb-000079
Figure PCTCN2022088560-appb-000080
-SCH 3、-N(CH 3) 2、
Figure PCTCN2022088560-appb-000081
Figure PCTCN2022088560-appb-000075
Figure PCTCN2022088560-appb-000076
-OCH 2 CH 2 CH 3 , -OCH 2 CH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 CH 2 OH,
Figure PCTCN2022088560-appb-000077
Figure PCTCN2022088560-appb-000078
-OCH 2 CH 2 NC(O)CH 3 , -OCH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 OH,
Figure PCTCN2022088560-appb-000079
Figure PCTCN2022088560-appb-000080
-SCH 3 , -N(CH 3 ) 2 ,
Figure PCTCN2022088560-appb-000081
z为1或者2；z is 1 or 2;
x为1或者2；x is 1 or 2;
A 1选自
Figure PCTCN2022088560-appb-000082
Figure PCTCN2022088560-appb-000083
Figure PCTCN2022088560-appb-000084
A 1 is selected from
Figure PCTCN2022088560-appb-000082
Figure PCTCN2022088560-appb-000083
Figure PCTCN2022088560-appb-000084
R 2选自：氢、羟基、氧代基、氰基、环丙基、1，1-二甲基环丙基、-C(＝CH 2)CH 3、-C(CH 3)(＝CH 2)CH 3、-CH＝CH(CH 2) 2CH 3、-CH＝CHCH 3、-CH＝CH-环丙基、-C(O)NH 2、三氟甲基、甲基、三氟甲氧基、-C(O)OCH 3、-S(O) 2CH 3、-OCH 3、-CH 2NH 2或卤素(F、Cl、Br)； R 2 is selected from: hydrogen, hydroxyl, oxo, cyano, cyclopropyl, 1,1-dimethylcyclopropyl, -C(=CH 2 )CH 3 , -C(CH 3 )(=CH 2 ) CH 3 , -CH=CH(CH 2 ) 2 CH 3 , -CH=CHCH 3 , -CH=CH-cyclopropyl, -C(O)NH 2 , trifluoromethyl, methyl, trifluoro Methoxy, -C(O) OCH3 , -S(O) 2CH3 , -OCH3 , -CH2NH2 or halogen ( F, Cl , Br);
w为1、2或者3；w is 1, 2 or 3;
A 2选自
Figure PCTCN2022088560-appb-000085
Figure PCTCN2022088560-appb-000086
A 2 selected from
Figure PCTCN2022088560-appb-000085
Figure PCTCN2022088560-appb-000086
R 3选自-C(O)NH(CH 2) 2CH 3、-C(O)N(CH 3) 2、-C(O)NH 2、-C(O)NH(CH 2) 2N(CH 3) 2、-CH 2C(O)NH 2、氢、-F、-Cl、-Br、氰基、-CF 3、-CH 3、-CH 2CH 3、-CH＝CH 2、-CH 2CN、-CH(CH 3)-NH 2、-CH＝CH-CN、-C(O)-OH、-C(O)OCH 3、-C(O)CH 3、-C(CH 3) 2-C(O)-OCH 3、-C(CH 3) 2-CN、氧代基、羟基、环丙基、环丁基、环戊基、-NH 2、-NH-C(O)CH 3、-NH-S(O) 2CH 3、-NH-C(O)OC(CH 3) 3、
Figure PCTCN2022088560-appb-000087
Figure PCTCN2022088560-appb-000088
-S(O) 2CH 3、-S(O) 2NCH 3、-S(O) 2NH 2、-OCH 2CH 3、-O(CH 2) 2CH 3、-OCF 3、
Figure PCTCN2022088560-appb-000089
-OCH 2环丙基、-OCH 3、-O(CH 2) 3CH 3、-OCH 2苯基、-O-苯基、-(CH 2)-OH、-(CH 2) 2-OH、-(CH 2)-OCH 3、-(CH 2)-OCH 2CH 3、-CH(OH)-CH 2-苯基、-CH(OH)-CH 2CH 3、-CH(OH)-CH 2CH 2CH 3、-CH(OH)-CH 2CH 2CH 2CH 3、-CH(OH)-CH(CH 3) 2、-CH(OH)-苯基、-CH(OH)-CN、-CH(OH)-CH 2-OH、-CH(OH)-CF 3、-CH(OH)-(CH 2) 2-苯基、 ＊-CH(OH)-C≡CH、-CH(NH 2)-CH 2-C(O)OH、-CH 2-NH-S(O) 2-CH 3、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2、-CH 2-NH-CH 2CH 3、-CH(CH 3)-NH 2、-CH 2-NH 2、-CH 2CH 2-NH 2、-CH 2NH-CH 2-苯基、-CH 2N(CH 2CH 3) 2、-CH 2NH-环丙基、-CH 2NH-环丁基、-CH 2NH-环戊基、-CH 2NH-吡啶基、-CH 2NH-苯基、-CH 2NH-(CH 2) 2-OH、-CH 2N(CH 3)-(CH 2) 2-OH、-CH 2NH-CH 2-CN、-CH 2N(CH 3)-CH 2-CN、-CH 2N(CH 3)-CH 2- CF 3、-CH 2N(CH 3)-CH 2-CF 2H、-CH 2NH-CH 2-CF 2H、-CH 2NH-(CH 2) 2-OCH 3、
Figure PCTCN2022088560-appb-000090
Figure PCTCN2022088560-appb-000091
Figure PCTCN2022088560-appb-000092
-CH 2NH-C(O)-OC(CH 3) 3、-CH 2CH 2NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 2NOH、-CH 2NH-C(O)-CH 2OCH 3、-CH(CH 3)NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 3、
Figure PCTCN2022088560-appb-000093
-CH 2NHCH 2-C(O)-NH 2、-CH 2NHCH 2-C(O)-(CH 3) 2、-CH 2NHCH 2-C(O)-OCH 3、-CH 2NHCH 2-C(O)-NHCH 3、-CH 2NHCH 2-C(O)-NH(CH 2) 2-OCH 3、-CH 2NHCH 2-C(O)-NHCH 2-苯基、
Figure PCTCN2022088560-appb-000094
-CH 2NHCH 2-C(O)-NH-苯基、
Figure PCTCN2022088560-appb-000095
-CH 2NH-C(O)-CH 2NH-苯基、
Figure PCTCN2022088560-appb-000096
或-CH 2NH-C(O)-CH 2NH-CH 2CF 3； R3 is selected from -C(O)NH( CH2 ) 2CH3 , -C(O)N( CH3 ) 2 , -C(O) NH2 , -C (O)NH( CH2 ) 2N (CH 3 ) 2 , -CH 2 C(O)NH 2 , hydrogen, -F, -Cl, -Br, cyano, -CF 3 , -CH 3 , -CH 2 CH 3 , -CH=CH 2 , -CH 2 CN, -CH(CH 3 )-NH 2 , -CH=CH-CN, -C(O)-OH, -C(O)OCH 3 , -C(O)CH 3 , -C(CH 3 ) 2 -C(O)-OCH 3 , -C(CH 3 ) 2 -CN, oxo, hydroxyl, cyclopropyl, cyclobutyl, cyclopentyl, -NH 2 , -NH-C(O )CH 3 , -NH-S(O) 2 CH 3 , -NH-C(O)OC(CH 3 ) 3 ,
Figure PCTCN2022088560-appb-000087
Figure PCTCN2022088560-appb-000088
-S(O) 2 CH 3 , -S(O) 2 NCH 3 , -S(O) 2 NH 2 , -OCH 2 CH 3 , -O(CH 2 ) 2 CH 3 , -OCF 3 ,
Figure PCTCN2022088560-appb-000089
-OCH 2 cyclopropyl, -OCH 3 , -O(CH 2 ) 3 CH 3 , -OCH 2 phenyl, -O-phenyl, -(CH 2 )-OH, -(CH 2 ) 2 -OH, -(CH 2 )-OCH 3 , -(CH 2 )-OCH 2 CH 3 , -CH(OH)-CH 2 -phenyl, -CH(OH)-CH 2 CH 3 , -CH(OH)-CH 2CH2CH3 , -CH(OH ) -CH2CH2CH2CH3 , -CH(OH ) -CH ( CH3 ) 2 , -CH(OH ) -phenyl, -CH(OH)-CN , -CH(OH)-CH 2 -OH, -CH(OH)-CF 3 , -CH(OH)-(CH 2 ) 2 -phenyl, * -CH(OH)-C≡CH, -CH( NH 2 )-CH 2 -C(O)OH, -CH 2 -NH-S(O) 2 -CH 3 , -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 , -CH 2 -NH-CH 2 CH 3 , -CH(CH 3 )-NH 2 , -CH 2 -NH 2 , -CH 2 CH 2 -NH 2 , - CH2NH - CH2 -phenyl, -CH2N(CH2CH3)2 , -CH2NH - cyclopropyl , -CH2NH - cyclobutyl, -CH2NH - cyclopentyl, - CH2NH -pyridyl, -CH2NH-phenyl, -CH2NH-( CH2 ) 2 -OH, -CH2N ( CH3 )-( CH2 ) 2 - OH, -CH2NH- CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CF 3 , -CH 2 N(CH 3 )-CH 2 -CF 2 H, -CH 2 NH-CH 2 -CF 2 H, -CH 2 NH-(CH 2 ) 2 -OCH 3 ,
Figure PCTCN2022088560-appb-000090
Figure PCTCN2022088560-appb-000091
Figure PCTCN2022088560-appb-000092
-CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 2 NOH, -CH 2 NH-C(O)-CH 2 OCH 3 , -CH(CH 3 )NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 3 ,
Figure PCTCN2022088560-appb-000093
-CH 2 NHCH 2 -C(O)-NH 2 , -CH 2 NHCH 2 -C(O)-(CH 3 ) 2 , -CH 2 NHCH 2 -C(O)-OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 3 , -CH 2 NHCH 2 -C(O)-NH(CH 2 ) 2 -OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 2 -phenyl,
Figure PCTCN2022088560-appb-000094
-CH 2 NHCH 2 -C(O)-NH-phenyl,
Figure PCTCN2022088560-appb-000095
-CH 2 NH-C(O)-CH 2 NH-phenyl,
Figure PCTCN2022088560-appb-000096
or -CH 2 NH-C(O)-CH 2 NH-CH 2 CF 3 ;
Y为1或者2；Y is 1 or 2;
L'为键、-(CH 2) k-或者-O(CH 2) k-，所述k为1或者2，或者L'为-CH＝CH-(CH 2) n,所述n为0或者1。 L' is a bond, -(CH 2 ) k - or -O(CH 2 ) k -, the k is 1 or 2, or L' is -CH=CH-(CH 2 ) n , the n is 0 or 1.
更优选的，本发明某些实施方式中，所述S2为WO2019201848A1(其全文通过引用的方式并入本文中)中实施例1(Example 1)至实施例100(Example 100)的具体化合物。More preferably, in certain embodiments of the present invention, the S2 is the specific compound of Example 1 (Example 1) to Example 100 (Example 100) in WO2019201848A1 (the entirety of which is incorporated herein by reference).
本发明某些实施方式中，所述S2a中，w为1或者2。In some embodiments of the present invention, in the S2a, w is 1 or 2.
本发明某些实施方式中，所述S2a中，R 1为氢、甲基、-OCH 3、-OCH 2CH 3、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2 或-O(CH 2) 3CH 3，例如-OCH 3。 In certain embodiments of the present invention, in the S2a, R 1 is hydrogen, methyl, -OCH 3 , -OCH 2 CH 3 , -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 or -O(CH 2 ) 3 CH 3 , eg -OCH 3 .
本发明某些实施方式中，所述S2a中，A 1为
Figure PCTCN2022088560-appb-000097
In some embodiments of the present invention, in the S2a, A 1 is
Figure PCTCN2022088560-appb-000097
本发明某些实施方式中，所述S2a中，A 1为
Figure PCTCN2022088560-appb-000098
In some embodiments of the present invention, in the S2a, A 1 is
Figure PCTCN2022088560-appb-000098
本发明某些实施方式中，所述S2a中，R 2为氢、卤素、-NH 2、C 1-C 6烷基或-C 1-C 6卤代烷基。 In certain embodiments of the present invention, in the S2a, R 2 is hydrogen, halogen, -NH 2 , C 1 -C 6 alkyl or -C 1 -C 6 haloalkyl.
本发明某些实施方式中，所述S2a中，L'为键。In some embodiments of the present invention, in the S2a, L' is a bond.
本发明某些实施方式中，所述S2a中，A 2(R 3) Y为氢。 In certain embodiments of the present invention, in the S2a, A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S2a中，A 2为
Figure PCTCN2022088560-appb-000099
In some embodiments of the present invention, in the S2a, A 2 is
Figure PCTCN2022088560-appb-000099
本发明某些实施方式中，所述S2a中，R 3为氢、-F、-Cl、-Br、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2或-CH 2-NH-CH 2CH 3。 In some embodiments of the present invention, in the S2a, R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH2 -N( CH3 ) 2 or -CH2 -NH - CH2CH3 .
本发明某些实施方式中，所述S2a中，R 3为氢、Cl、-CH 2NHCH 3或-CH 2N(CH 3) 2。 In some embodiments of the present invention, in the S2a, R 3 is hydrogen, Cl, -CH 2 NHCH 3 or -CH 2 N(CH 3 ) 2 .
本发明某些实施方式中，所述S2a中，A 1为
Figure PCTCN2022088560-appb-000100
L'为键，A 2(R 3) Y为氢。 In some embodiments of the present invention, in the S2a, A 1 is
Figure PCTCN2022088560-appb-000100
L' is a bond, and A 2 (R 3 ) Y is hydrogen.
本发明某些实施方式中，所述S2a中，A 1为
Figure PCTCN2022088560-appb-000101
L'为键，A 2为
Figure PCTCN2022088560-appb-000102
R 3为氢、-F、-Cl、-Br、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2或-CH 2-NH-CH 2CH 3。 In some embodiments of the present invention, in the S2a, A 1 is
Figure PCTCN2022088560-appb-000101
L' is the key, A 2 is
Figure PCTCN2022088560-appb-000102
R 3 is hydrogen, -F, -Cl, -Br, -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 or -CH 2 -NH - CH2CH3 .
本发明某些实施方式中，所述S为S2a'，In some embodiments of the present invention, the S is S2a',
Figure PCTCN2022088560-appb-000103
Figure PCTCN2022088560-appb-000103
其中，所述S2a'中，T、V、R 1、R 2、R 3、L'、A 1、A 2、w、x和Y的定义如S2或S2a中所述。 Wherein, in the S2a', the definitions of T, V, R 1 , R 2 , R 3 , L', A 1 , A 2 , w, x and Y are as described in S2 or S2a.
本发明某些实施方式中，所述S为S2a”，In some embodiments of the present invention, the S is S2a",
Figure PCTCN2022088560-appb-000104
Figure PCTCN2022088560-appb-000104
其中，所述S2a”中，T、V、R 2、R 3、L'、A 1、A 2、w和Y的定义如S2或S2a中所述。 Wherein, in the S2a", the definitions of T, V, R 2 , R 3 , L', A 1 , A 2 , w and Y are as described in S2 or S2a.
本发明某些实施方式中，所述S2a'、S2a”中，R 1为氢、C 1-C 6烷基或C 1-C 6烷氧基，所述C 1-C 6烷基和C 1-C 6烷氧基任选的被C 1-C 6烷氧基(例如甲氧基)取代。 In certain embodiments of the present invention, in the S2a', S2a", R 1 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 alkoxy, the C 1 -C 6 alkyl and C 1 -C6alkoxy is optionally substituted with C1 - C6alkoxy (eg methoxy).
本发明某些实施方式中，所述S2a'、S2a”中，R 1为氢、甲基、甲氧基或
Figure PCTCN2022088560-appb-000105
In certain embodiments of the present invention, in the S2a', S2a", R 1 is hydrogen, methyl, methoxy or
Figure PCTCN2022088560-appb-000105
本发明某些实施方式中，所述S2a、S2a'、S2a”中，
Figure PCTCN2022088560-appb-000106
片段为
Figure PCTCN2022088560-appb-000107
In some embodiments of the present invention, in the S2a, S2a', S2a",
Figure PCTCN2022088560-appb-000106
Fragment is
Figure PCTCN2022088560-appb-000107
本发明某些实施方式中，所述S为-X-S2a'，S2a'的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S2a', and the structure of S2a' is as described above; X is O, NH or S, preferably O.
本发明某些实施方式中，所述S为-X-S2a”，S2a”的结构如上所述；X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S2a", and the structure of S2a" is as described above; X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S3：Preferably, in some embodiments of the present invention, the S is S3:
Figure PCTCN2022088560-appb-000108
Figure PCTCN2022088560-appb-000108
其中所述S3中：where the S3:
Q 1和Q 2各自独立的CH或者N； Q 1 and Q 2 are each independent CH or N;
Q 3、Q 4和Q 7各自独立的为C或者N，所述Q 3和Q 4至少有一个为C，所述Q 3、Q 4和Q 7不全部为N； Q 3 , Q 4 and Q 7 are independently C or N, at least one of said Q 3 and Q 4 is C, and not all of said Q 3 , Q 4 and Q 7 are N;
Q 5为CH、N、NH、O或者S； Q 5 is CH, N, NH, O or S;
Q 6为CH、N、NH、N(C 1-C 6烷基)、N(C 1-C 6杂烷基)、N(3-7元环烷基)、N(3-7元杂环)、O或者S； Q 6 is CH, N, NH, N(C 1 -C 6 alkyl), N(C 1 -C 6 heteroalkyl), N(3-7 membered cycloalkyl), N(3-7 membered heteroalkyl) ring), O or S;
所述Q 1、Q 2、Q 3、Q 4、Q 5、Q 6和Q 7中至少有一个为N、NH、O或者S； At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 , Q 6 and Q 7 is N, NH, O or S;
R 1选自氢、C 1-C 6烷基、C 1-C 6烷氧基、卤素、-NHR 1a、-OR 1a、C 3-C 6环烷基、C 3-C 6环烷氧基或者-CN；所述C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基和C 3-C 6环烷氧基任选的被选自卤素、-NHR 1a或-OR 1a的取代基取代；所述R 1a为氢、C 1-C 6烷基、3-6元杂环或者C 1-C 6卤代烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, halogen, -NHR 1a , -OR 1a , C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or -CN; the C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl and C 3 -C 6 cycloalkoxy are optionally selected from halogen, Substituent substitution of -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-S(O)-、-S(＝O)(＝NH)-、-S(＝O)[＝N(C 1-C 6烷基)]-、-N(C 1-C 6烷基)-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -S(O)-, - S(=O)(=NH)-, -S(=O)[=N(C 1 -C 6 alkyl)]-, -N(C 1 -C 6 alkyl)-, -C(O) (CH 2 ) p -, -(CH 2 ) p - or O; the o is 0, 1 or 2; the p is an integer from 1 to 6;
R 2选自氢、卤素、-CN、-NO 2、C 1-C 6烷基巯基、C 2-C 6炔基、C 1-C 6烷基、C 2-C 6烯基、-NR 2bR 2c、-OR 2a、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述C 1-C 6烷基、C 2-C 6烯基、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、C 1-C 6卤代烷基、-OH、-OR 2a、氧代基、卤素、-C(O)R 2a、-C(O)OR 2a、-C(O)NR 2bR 2c、-CN、-NR 2bR 2c、3-6元环烷基、3-7元杂环烷基、6-10元芳基或5-10元杂芳基的取代基取代；所述R 2a为氢、C 1-C 6烷基、C 1-C 6卤代烷基、3-7元杂环烷基、或者-(CH 2) rOCH 3，所述r为1、2或者3； R 2 is selected from hydrogen, halogen, -CN, -NO 2 , C 1 -C 6 alkylmercapto, C 2 -C 6 alkynyl, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, -NR 2b R 2c , -OR 2a , 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-10-membered heteroaryl; the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5- The 10-membered heteroaryl groups are each independently optionally selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, -OH, -OR 2a , oxo, halogen, -C(O)R 2a , -C(O)OR 2a , -C(O)NR 2b R 2c , -CN, -NR 2b R 2c , 3-6-membered cycloalkyl, 3-7-membered heterocycloalkyl, 6-10-membered aryl substituted with a 5- to 10-membered heteroaryl group; the R 2a is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, 3-7 membered heterocycloalkyl, or -(CH 2 ) r OCH 3 , the r is 1, 2 or 3;
所述R 2b为氢或C 1-C 6烷基； The R 2b is hydrogen or C 1 -C 6 alkyl;
所述R 2c为氢或C 1-C 6烷基； The R 2c is hydrogen or C 1 -C 6 alkyl;
R 2为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b,所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基(例如，所述R a和R b各自独立的为氢或C 1-C 6烷基)； R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, C 1 -C 6 alkyl , C 3 -C 8 heterocycloalkyl, or C 3 -C 8 cycloalkyl (eg, the R a and R b are each independently hydrogen or C 1 -C 6 alkyl);
R 2为-NH-(CH 2) k-NH-C(O)-(C 1-C 6烷基)，所述k为1或者2； R 2 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
R 2为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
R 3和R 4各自独立的为氢、C 1-C 6烷基、C 1-C 6烷氧基或C 3-C 6环烷氧基；所述R 3和R 4至少有一个不为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基；所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代； R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or C 3 -C 6 cycloalkoxy; at least one of said R 3 and R 4 is not hydrogen, or the R 3 and R 4 and the atoms to which they are attached together form a 3-6 membered cycloalkyl; the alkyl, alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or halogen substituted;
A为任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)6-元芳基或者任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)5-6元杂芳基。 A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 Substituted, R2 is as defined in S1 ) 5-6 membered heteroaryl.
优选的，本发明某些实施方式中，所述S为S3a，Preferably, in some embodiments of the present invention, the S is S3a,
Figure PCTCN2022088560-appb-000109
Figure PCTCN2022088560-appb-000109
其中所述S3a中：Where said S3a:
Q 1和Q 2各自独立的CH或者N； Q 1 and Q 2 are each independent CH or N;
Q 3和Q 4各自独立的为C或者N，所述Q 3和Q 4至少有一个为C； Q 3 and Q 4 are independently C or N, and at least one of the Q 3 and Q 4 is C;
Q 6为CH、N、NH、O或者S； Q 6 is CH, N, NH, O or S;
Q 5为CH、N、NH、O或者S； Q 5 is CH, N, NH, O or S;
所述Q 1、Q 2、Q 3、Q 4、Q 5和Q 6中至少有一个为N、NH、O或者S； At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 and Q 6 is N, NH, O or S;
R 1选自氢、C 1-C 6烷基、卤素、-OR 1a、环丙基或者-CN；所述R 1a为氢或C 1-C 6烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -OR 1a , cyclopropyl or -CN; said R 1a is hydrogen or C 1 -C 6 alkyl;
L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
R 2选自氢、-(CH 2) qCH 3、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述q为1至5的整数；所述3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、-OH、卤素、-C(O)R 2a、-C(O)NR 2bR 2c的取代基取代；所述R 2a为C 1-C 6烷基或者-(CH 2) rOCH 3，所述r为1、2或者3；所述R 2b为氢或C 1-C 6烷基；所述R 2c为氢或C 1-C 6烷基； R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; said q is an integer from 1 to 5; said 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5 -10-membered heteroaryl groups are each independently optionally substituted with a substituent selected from C 1 -C 6 alkyl, -OH, halogen, -C(O)R 2a , -C(O)NR 2b R 2c ; The R 2a is C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 , the r is 1, 2 or 3; the R 2b is hydrogen or C 1 -C 6 alkyl; the R 2c is hydrogen or C 1 -C 6 alkyl;
R 3和R 4各自独立的为氢或C 1-C 6烷基，所述R 3和R 4至少有一个不为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is not hydrogen, or said R 3 and R 4 together with the atoms to which they are attached form 3 -6-membered cycloalkyl;
A为任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)苯基或者任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)5-6元杂芳基。 A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) phenyl or optionally substituted (eg optionally substituted with 1 or more R2, R2 2 is as defined in S1) 5-6 membered heteroaryl.
更优选的，本发明某些实施方式中，所述S3为WO2020180768A1(其全文通过引用的方式并入本文中)中实施例1(Example 1)至实施例103(Example 103)的具体化合物。More preferably, in certain embodiments of the present invention, the S3 is a specific compound of Example 1 (Example 1) to Example 103 (Example 103) in WO2020180768A1 (the entirety of which is incorporated herein by reference).
优选的，本发明某些实施方式中，所述S为S4：Preferably, in some embodiments of the present invention, the S is S4:
Figure PCTCN2022088560-appb-000110
Figure PCTCN2022088560-appb-000110
其中所述S4中：Where the S4:
Q 1为CH或者N； Q 1 is CH or N;
Q 4为CH、C或者N； Q 4 is CH, C or N;
每个Q 2各自独立的为C-R 1或者N，所述Q 2其中一个为N另一个Q 2为C-R 1； Each Q 2 is independently CR 1 or N, and one of the Q 2 is N and the other Q 2 is CR 1 ;
每个Q 3和Q 5分子独立的为C(R QC) 2、NR QN、C(O)、O、S或者SO 2，所述R QC各自独立的为氢、 F、Cl、Br、或者6-10元芳基，所述R QN各自独立的为氢、C 1-C 6烷基或者6-10元芳基； Each Q 3 and Q 5 molecule is independently C(R QC ) 2 , NR QN , C(O), O, S, or SO 2 , and each R QC is independently hydrogen, F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
所述Q 1、Q 2、Q 3、Q 4、和Q 5至少有一个是N、NR QN、O或者SO 2； At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
m为0、1、2或者3；m is 0, 1, 2 or 3;
n为0、1、2或者3；n is 0, 1, 2 or 3;
且当m为0时，n不是0；And when m is 0, n is not 0;
R 1选自氢、C 1-C 6烷基、卤素、-C(O)NHR 1a、-NHR 1a、-OR 1a、环丙基、氮杂环丁烷或者-CN；所述C 1-C 6烷基和氮杂环丁烷任选的被选自卤素、R 1a、-NHR 1a或-OR 1a的取代基取代；所述R 1a为氢、C 1-C 6烷基、环丙基、3-6元杂环或者C 1-C 6卤代烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -C(O)NHR 1a , -NHR 1a , -OR 1a , cyclopropyl, azetidine or -CN; the C 1 - C6 alkyl and azetidine are optionally substituted with substituents selected from halogen, R 1a , -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, cyclopropyl base, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-S(O)-、-S(＝O)(＝NH)-、-S(＝O)[＝N(C 1-C 6烷基)]-、-N(C 1-C 6烷基)-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -S(O)-, - S(=O)(=NH)-, -S(=O)[=N(C 1 -C 6 alkyl)]-, -N(C 1 -C 6 alkyl)-, -C(O) (CH 2 ) p -, -(CH 2 ) p - or O; the o is 0, 1 or 2; the p is an integer from 1 to 6;
R 2选自氢、C 1-C 6烷基、-NR 2bR 2c、-OR 2a、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述C 1-C 6烷基、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基、C 1-C 6甲氧基烷基、-OH、-OR 2a、氧代基、卤素、＝N、-C(O)R 2a、-C(O)OR 2a、-C(O)NR 2bR 2c、-S(O) 2R 2a、-CN、-NR 2bR 2c、3-6元环烷基、3-7元杂环烷基、6-10元芳基或5-10元杂芳基的取代基取代；所述R 2a为氢、C 1-C 6烷基、C 1-C 6卤代烷基、3-7元杂环烷基、或者-(CH 2) rOCH 3，所述r为1、2或者3； R 2 is selected from hydrogen, C 1 -C 6 alkyl, -NR 2b R 2c , -OR 2a , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6 -10-membered aryl, 5-10-membered heteroaryl; the C 1 -C 6 -membered alkyl, 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-membered -10-membered aryl and 5-10-membered heteroaryl are each independently optionally selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl, C 1 - C 6methoxyalkyl , -OH, -OR 2a , oxo, halogen, =N, -C(O)R 2a , -C(O)OR 2a , -C(O)NR 2b R 2c , -S(O) 2 R 2a , -CN, -NR 2b R 2c , 3-6 membered cycloalkyl, 3-7 membered heterocycloalkyl, 6-10 membered aryl or 5-10 membered heteroaryl Substituent substitution; the R 2a is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, 3-7 membered heterocycloalkyl, or -(CH 2 ) r OCH 3 , and the r is 1, 2 or 3;
所述R 2b为氢或C 1-C 6烷基； The R 2b is hydrogen or C 1 -C 6 alkyl;
所述R 2c为氢或C 1-C 6烷基； The R 2c is hydrogen or C 1 -C 6 alkyl;
R 3和R 4各自独立的为氢、任选被卤素、-OH取代的C 1-C 6烷基，所述R 3和R 4至少有一个为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl optionally substituted by halogen, -OH, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and The atoms to which it is attached together form a 3-6 membered cycloalkyl;
A为任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)6-元芳基或者任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)5-6元杂芳基； A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 substituted, R is as defined in S1 ) 5-6 membered heteroaryl;
条件是当
Figure PCTCN2022088560-appb-000111
为
Figure PCTCN2022088560-appb-000112
Figure PCTCN2022088560-appb-000113
Figure PCTCN2022088560-appb-000114
或者
Figure PCTCN2022088560-appb-000115
时，R 1不为氢。 condition is when
Figure PCTCN2022088560-appb-000111
for
Figure PCTCN2022088560-appb-000112
Figure PCTCN2022088560-appb-000113
Figure PCTCN2022088560-appb-000114
or
Figure PCTCN2022088560-appb-000115
, R 1 is not hydrogen.
优选的，本发明某些实施方式中，所述S为S4aPreferably, in some embodiments of the present invention, the S is S4a
Figure PCTCN2022088560-appb-000116
Figure PCTCN2022088560-appb-000116
其中所述S4a中：Where said S4a:
Q 1为CH或者N； Q 1 is CH or N;
Q 4为CH、C或者N； Q 4 is CH, C or N;
每个Q 2各自独立的为CR 1或者N； Each Q 2 is independently CR 1 or N;
每个Q 3和Q 5分子独立的为C(R QC) 2、NR QN、C(O)、O、S或者SO 2，所述R QC各自独立的为氢、F、Cl、Br、或者6-10元芳基，所述R QN各自独立的为氢、C 1-C 6烷基或者6-10元芳基； Each Q3 and Q5 molecule is independently C( RQC ) 2 , NRQN , C(O), O, S, or SO2, and each RQC is independently hydrogen , F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
所述Q 1、Q 2、Q 3、Q 4、和Q 5至少有一个是N、NR QN、O或者SO 2； At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
R 1选自氢、C 1-C 6烷基、卤素、环丙基、氰基或-OR 1a，所述R 1a为氢或C 1-C 6烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, cyclopropyl, cyano or -OR 1a , said R 1a is hydrogen or C 1 -C 6 alkyl;
L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
R 2选自氢、-(CH 2) qCH 3、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述q为1至5的倍数；所述3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、羟基、卤素、-C(O)R 2a或-C(O)NR 2bR 2c的基团取代；所述R 2a选自C 1-C 6烷基或-(CH 2) rOCH 3；所述r为1、2或者3；所述R 2b和R 2c各自独立的为氢或C 1-C 6烷基； R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; the q is a multiple of 1 to 5; the 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-membered -10-membered heteroaryl groups are each independently optionally substituted with a group selected from C 1 -C 6 alkyl, hydroxy, halogen, -C(O)R 2a or -C(O)NR 2b R 2c ; the The R 2a is selected from C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 ; the r is 1, 2 or 3; the R 2b and R 2c are each independently hydrogen or C 1 -C 6 alkyl;
R 3和R 4各自独立的为氢或C 1-C 6烷基，所述R 3和R 4至少有一个为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and the atoms to which they are attached together form a 3- 6-membered cycloalkyl;
A为任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)6-元芳基或者任选取代的(例如任选1个或多个R 2取代，R 2的定义如S1中所述)5-6元杂芳基。 A is optionally substituted (eg optionally substituted with 1 or more R2, R2 is as defined in S1) 6 -membered aryl or optionally substituted (eg optionally substituted with 1 or more R2 Substituted, R2 is as defined in S1 ) 5-6 membered heteroaryl.
优选的，本发明某些实施方式中，所述S4a中R 3和R 4各自独立的为氢或甲基，所述R 3和R 4至少有一个为氢。 Preferably, in some embodiments of the present invention, R 3 and R 4 in the S4a are each independently hydrogen or methyl, and at least one of the R 3 and R 4 is hydrogen.
更优选的，本发明某些实施方式中，所述S4为WO2020180770A1(其全文通过引用的方式并入本文中)中实施例1(Example 1)至实施例540(Example 540)的具体化合物。More preferably, in certain embodiments of the present invention, the S4 is the specific compound of Example 1 (Example 1) to Example 540 (Example 540) in WO2020180770A1 (which is incorporated herein by reference in its entirety).
优选的，本发明某些实施方式中，所述S为S5：Preferably, in some embodiments of the present invention, the S is S5:
Figure PCTCN2022088560-appb-000117
Figure PCTCN2022088560-appb-000117
其中所述S5中：Where said S5:
所述R 1为氢或R a1； The R 1 is hydrogen or R a1 ;
R a1选自C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 1-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10元芳基或者5-10元杂芳基，所述C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 1-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10元芳基和5-10元杂芳基任选的被1个或多个相同的或者不同的R b1和/或R c1取代； R a1 is selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 Cycloalkenyl, 3-10-membered heterocycloalkyl, C 6 -C 10 -membered aryl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 membered aryl and 5-10 membered heteroaryl is optionally substituted with one or more identical or different R b1 and/or R c1 ;
每个R b1各自独立的为-OR c1、-NR c1R c1、卤素、-CN、-C(O)R c1、-C(O)OR c1、-C(O)NR c1R c1、-S(O) 2R c1、-S(O) 2NR c1R c1、-NHC(O)R c1、-N(C 1-C 4烷基)C(O)R c1、-NHC(O)OR c1或者-N(C 1-C 4烷基)C(O)OR c1； Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4alkyl )C(O)R c1 , -NHC(O) OR c1 or -N(C 1 -C 4 alkyl)C(O)OR c1 ;
每个R c1各自独立的为氢、C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基或者5-10元杂芳基；所述C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基和5-10元杂芳基各自独立的任选的被1个或者多个相同的或者不同的R d1和/或R e1； Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl; the C 1 -C 6 alkyl, C 1 -C 6 Haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C The 10 -aryl and 5-10-membered heteroaryl groups are each independently optionally surrounded by 1 or more identical or different R d1 and/or R e1 ;
每个R d1各自的独立为-OR e1、-NR e1R e1、卤素、-CN、-C(O)R e1、-C(O)OR e1、-C(O)NR e1R e1、-S(O) 2R e1、-S(O) 2NR e1R e1、-NHC(O)R e1、-N(C 1-C 4烷基)C(O)R e1、-NHC(O)OR e1或者-N(C 1-C 4烷基)C(O)OR e1； Each R d1 is independently -OR e1 , -NR e1 R e1 , halogen, -CN, -C(O)R e1 , -C(O)OR e1 , -C(O)NR e1 R e1 , - S(O) 2 R e1 , -S(O) 2 NR e1 R e1 , -NHC(O)R e1 , -N(C 1 -C 4 alkyl)C(O)R e1 , -NHC(O) OR e1 or -N(C 1 -C 4 alkyl)C(O)OR e1 ;
每个R e1各自独立的为氢、C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基或者5-10元杂芳基； Each R e1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl;
R 2选自氢、C 1-C 4烷基、C 3-C 6环烷基、3-6元杂环烷基或者卤素； R 2 is selected from hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl or halogen;
环A选自C 6-C 10芳基、5-10元杂芳基或者9-10元双杂环烷基； Ring A is selected from C 6 -C 10 aryl, 5-10 membered heteroaryl or 9-10 membered biheterocycloalkyl;
p为1、2或3；p is 1, 2 or 3;
每个R 4各自独立的为氢、羟基、氧代、卤素、氰基、C 1-C 4烷基、-NH 2、C 1-C 4卤代烷基、C 2-C 4烯基、C 2-C 4炔基、C 1-C 4羟基烷基、羟基-C 1-C 4卤代烷基、C 3-C 6环烷基、C 3-C 6环烷氧基、3-6元杂环烷基、C 3-C 6羟基环烷基，被3-6元杂环烷基取代的C 1-C 4卤代烷基，被羟基、卤素、-NH 2、-S(O) 2-(C 1-C 4烷基)或者氧代基取代的3-6元杂环烷基，且氧代基仅在非芳香环上取代； Each R 4 is independently hydrogen, hydroxy, oxo, halogen, cyano, C 1 -C 4 alkyl, -NH 2 , C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy, 3-6 membered heterocycle Alkyl, C 3 -C 6 hydroxycycloalkyl, C 1 -C 4 haloalkyl substituted by 3-6 membered heterocycloalkyl, substituted by hydroxy, halogen, -NH 2 , -S(O) 2 -(C 1 -C 4 alkyl) or oxo-substituted 3-6 membered heterocycloalkyl, and the oxo group is only substituted on a non-aromatic ring;
R 4为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 4 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 4为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 4 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
R 4为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 4 is -C(O)OR g , and said R g is hydrogen or C 1 -C 6 alkyl;
R 4为-OR h；所述R h为C 1-C 6烷基； R 4 is -OR h ; Described R h is C 1 -C 6 alkyl;
或者R 4为-(CH 2)NR aR b，所述R a和R b各自独立的氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； or R 4 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
R 3和R 5各自独立的为氢、C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代。 R 3 and R 5 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkane radical, alkoxy, cycloalkyl and cycloalkoxy optionally by cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen substituted.
优选的，本发明某些实施方式中，所述S5中R 5为甲基。 Preferably, in some embodiments of the present invention, R 5 in the S5 is methyl.
在一些实施方案中，所述S5各基团的定义中，所述R a和R b在任一处出现时各自独立的为氢或C 1-C 6烷基。 In some embodiments, in the definition of each of the groups of S5, the Ra and Rb at any one occurrence are each independently hydrogen or C1 - C6 alkyl.
本发明某些实施方式中，所述S为S5'：In some embodiments of the present invention, the S is S5':
Figure PCTCN2022088560-appb-000118
Figure PCTCN2022088560-appb-000118
其中所述S5'中，所述R 2、R 3、R 4、R 5、环A和p如S5中所定义和描述。 wherein in said S5', said R 2 , R 3 , R 4 , R 5 , ring A and p are as defined and described in S5.
本发明某些实施方式中，所述S为-X-S5'，S5'的结构如上所述；X为O、NH或S，优选为O。In some embodiments of the present invention, the S is -X-S5', and the structure of S5' is as described above; X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S5a：Preferably, in some embodiments of the present invention, the S is S5a:
Figure PCTCN2022088560-appb-000119
Figure PCTCN2022088560-appb-000119
其中，所述R 1、R 2、R 3、R 4、环A和p如S5中所定义和描述。 wherein the R 1 , R 2 , R 3 , R 4 , ring A and p are as defined and described in S5.
本发明某些实施方式中，所述S为S5a'：In some embodiments of the present invention, the S is S5a':
Figure PCTCN2022088560-appb-000120
Figure PCTCN2022088560-appb-000120
其中所述S5a'中，所述R 2、R 3、R 4、R 5、环A和p如S5a中所定义和描述。 wherein in said S5a', said R 2 , R 3 , R 4 , R 5 , ring A and p are as defined and described in S5a.
本发明某些实施方式中，所述S为-X-S5a'，S5a'的结构如上所述；X为O、NH或S，优选为O。In some embodiments of the present invention, the S is -X-S5a', and the structure of S5a' is as described above; X is O, NH or S, preferably O.
更优选的，本发明某些实施方式中，所述S5为WO2019122129A1(其全文通过引用的方式并入本文中)中I-1至I-179的具体化合物。More preferably, in certain embodiments of the present invention, the S5 is a specific compound of I-1 to I-179 in WO2019122129A1 (which is incorporated herein by reference in its entirety).
优选的，本发明某些实施方式中，所述S为S6：Preferably, in some embodiments of the present invention, the S is S6:
Figure PCTCN2022088560-appb-000121
Figure PCTCN2022088560-appb-000121
其中所述S6中：Where said S6:
R 2选自氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 2选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基(例如
Figure PCTCN2022088560-appb-000122
)、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基(例如
Figure PCTCN2022088560-appb-000123
)、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环C烷 3-基C 8、环苯烷基基、或杂-芳C 4-基C、 8C环 1-烯C 6基；卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、R 2为-NS(O)(R d)(R e)，所述R d和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、6-10元芳基或5-10元杂芳基； R 2 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy (eg
Figure PCTCN2022088560-appb-000122
), C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl (eg
Figure PCTCN2022088560-appb-000123
), 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloC alkane 3 -yl C 8 , cyclophenylalkyl, or hetero-aryl C 4 -yl C, 8 C ring 1 -alkenyl C 6 group; haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, R 2 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 6-10 membered aryl or 5-10 membered heteroaryl;
R 2为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b，所述R a和R b各自独立的为氢、-C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , and said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 2为-NH-(CH 2) k-NH-C(O)-R aa，所述R aa为C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基，且k为1或者2； R 2 is -NH-(CH 2 ) k -NH-C(O)-R aa which is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl, and k is 1 or 2;
R 2为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b The group is substituted; the R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
R 2为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 2 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
或者R 2为 or R2 for
Figure PCTCN2022088560-appb-000124
Figure PCTCN2022088560-appb-000125
或者
Figure PCTCN2022088560-appb-000126
Figure PCTCN2022088560-appb-000124
Figure PCTCN2022088560-appb-000125
or
Figure PCTCN2022088560-appb-000126
R 1为氢或-OR A； R 1 is hydrogen or -OR A ;
R A为氢、C 3-C 10环烷基或3-10元杂环烷基；所述C 3-C 10环烷基和3-10元杂环烷基任选被1个或者多个相同或不同的R a1和/或R c1取代； R A is hydrogen, C 3 -C 10 cycloalkyl or 3-10 membered heterocycloalkyl; the C 3 -C 10 cycloalkyl and 3-10 membered heterocycloalkyl are optionally composed of one or more same or different R a1 and/or R c1 substitutions;
每个R a1各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基；所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基各自独立的任选的被1个或者多个相同或不同的R b1和/或R c1取代； Each R a1 is independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3 -10-membered heterocycloalkyl or 5-10-membered heteroaryl; said C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are each independently optionally substituted by one or more identical or different R b1 and/or R c1 ;
每个R b1各自独立的为-OR c1、-NR c1R c1、卤素、-CN、-C(O)R c1、-C(O)OR c1、-C(O)NR c1R c1、-S(O) 2R c1、-S(O) 2NR c1R c1、-NHC(O)R c1、-N(C 1-C 4烷基)C(O)R c1、氧代基所取代，且所述氧代基仅在非芳香环取代； Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4 alkyl)C(O)R c1 , oxo substituted , and the oxo group is only substituted on a non-aromatic ring;
每个R c1各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10杂芳基； Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl , 3-10 membered heterocycloalkyl or 5-10 heteroaryl;
或者R 1选自C 3-C 10环烷基、C 3-C 10环烯基、C 6-C 10芳基、3-10元杂环烷基或5-10元杂芳基；所述C 3-C 10环烷基、C 3-C 10环烯基、C 6-C 10芳基、3-10元杂环烷基或5-10元杂芳基任选的被1个或多个R a2和/或R b2取代； or R 1 is selected from C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl; the C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl are optionally surrounded by one or more R a2 and/or R b2 substitutions;
每个R a2各自独立的选自C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R c2和/或R b2取代； Each R a2 is independently selected from C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkane base, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl optionally substituted by 1 or more R c2 and/or R b2 ;
每个R b2各自独立的选自-OR c2、-NR c2R c2、卤素、-CN、-C(O)R c2、-C(O)OR c2、-C(O)NR  c2R c2、-OC(O)R c2、-S(O) 2R c2、-S(O) 2NR c2R c2、-NHC(O)R c2、-N(C 1-C 4烷基)C(O)R c2、-NHC(O)OR c2、氧代基、＝NH，且所述氧代基、＝NH仅在非芳香环上取代； Each R b2 is independently selected from -OR c2 , -NR c2 R c2 , halogen, -CN, -C(O)R c2 , -C(O)OR c2 , -C(O)NR c2 R c2 , -OC(O)R c2 , -S(O) 2 R c2 , -S(O) 2 NR c2 R c2 , -NHC(O)R c2 , -N(C 1 -C 4 alkyl)C(O ) R c2 , -NHC(O)OR c2 , oxo, =NH, and said oxo, =NH are only substituted on non-aromatic rings;
每个R c2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R d2和/或R e2取代； Each R c2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d2 and/or R e2 ;
每个R d2各自独立的为-OR e2、-NR e2R e2、卤素、-CN、-C(O)R e2、-C(O)OR e2、-C(O)NR e2R e2、-S(O) 2R e2、-S(O) 2NR e2R e2、-NHC(O)R e2、-N(C 1-C 4烷基)C(O)R e2、氧代基，所述氧代基仅在非芳香环上取代； Each R d2 is independently -OR e2 , -NR e2 Re2 , halogen, -CN, -C(O)R e2 , -C(O)OR e2 , -C(O)NR e2 Re2 , - S(O) 2 R e2 , -S(O) 2 NR e2 R e2 , -NHC(O)R e2 , -N(C 1 -C 4 alkyl)C(O)R e2 , oxo, all The oxo group is only substituted on a non-aromatic ring;
每个R e2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R f2和/或R g2取代； Each R e2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R f2 and/or R g2 ;
每个R f2各自独立的选自-OR g2、-NR g2R g2、卤素、-CN、-C(O)R g2、-C(O)OR g2、-C(O)NR g2R g2、-S(O) 2R g2、-S(O) 2NR g2R g2、-NHC(O)R g2、-N(C 1-C 4烷基)C(O)R g2、氧代基，所述氧代基仅在非芳香环上取代； Each R f2 is independently selected from -OR g2 , -NR g2 R g2 , halogen, -CN, -C(O)R g2 , -C(O)OR g2 , -C(O)NR g2 R g2 , -S(O) 2 R g2 , -S(O) 2 NR g2 R g2 , -NHC(O)R g2 , -N(C 1 -C 4 alkyl)C(O)R g2 , oxo, The oxo group is only substituted on a non-aromatic ring;
每个R g2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10 元杂环烷基或者5-10元杂芳基； Each R g2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
或R 1选自C 2-C 4烷基、C 2-C 4烯基；所述C 2-C 4烷基和C 2-C 4烯基任选的R b3取代； or R 1 is selected from C 2 -C 4 alkyl, C 2 -C 4 alkenyl; the C 2 -C 4 alkyl and C 2 -C 4 alkenyl are optionally substituted by R b3 ;
R b3选自-C(O)R c3、-C(O)OR c3、-C(O)NR c3R c3、-C(O)NHOR c3或者-C(O)N(C 1-C 4烷基)OR c3； R b3 is selected from -C(O)R c3 , -C(O)OR c3 , -C(O)NR c3 R c3 , -C(O)NHOR c3 or -C(O)N(C 1 -C 4 alkyl) OR c3 ;
每个R c3各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R d3和/或R e3取代； Each R c3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d3 and/or R e3 ;
每个R d3各自独立的选自-OR e3、-NR e3R e3、卤素、-CN、-C(O)R e3、-C(O)OR e3、-C(O)NR e3R e3、-S(O) 2R e3、-S(O) 2NR e3R e3、-NHC(O)R e3、-N(C 1-C 4烷基)C(O)R e3、氧代基，所述氧代基仅在非芳香环上取代； Each R d3 is independently selected from -OR e3 , -NR e3 R e3 , halogen, -CN, -C(O)R e3 , -C(O)OR e3 , -C(O)NR e3 R e3 , -S(O) 2 R e3 , -S(O) 2 NR e3 R e3 , -NHC(O)R e3 , -N(C 1 -C 4 alkyl)C(O)R e3 , oxo, The oxo group is only substituted on a non-aromatic ring;
每个R e3各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基； Each R e3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
R 3选自氢、C 1-C 4烷基、-O(C 1-C 4烷基)、-NH 2、-NH(C 1-C 4烷基)、-N(C 1-C 4烷基) 2或者卤素； R 3 is selected from hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl), -N(C 1 -C 4 alkyl) 2 or halogen;
R 5选自氢、羟基或者-NHR’； R 5 is selected from hydrogen, hydroxyl or -NHR';
R’选自氢、C 1-C 3烷基和-C(O)C 1-C 3烷基； R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
R 4选自C 1-C 4烷基、羟基、氧代、氰基、C 1-C 4烷氧基、C 1-C 4卤代烷基、C 1-C 4羟基烷基、羟基-C 1-C 4卤代烷基、C 2-C 6烯基、-C 2-C 6炔基、C 3-C 6环烷氧基、C 3-C 6环烷基、3-6元杂环烷基、3-6元羟基杂环烷基、卤素或者-SO 2-C 1-C 4烷基； R 4 is selected from C 1 -C 4 alkyl, hydroxy, oxo, cyano, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 2 -C 6 alkenyl, -C 2 -C 6 alkynyl, C 3 -C 6 cycloalkoxy, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl , 3-6 membered hydroxy heterocycloalkyl, halogen or -SO 2 -C 1 -C 4 alkyl;
R 6选自氢、C 1-C 4烷基或者卤素； R 6 is selected from hydrogen, C 1 -C 4 alkyl or halogen;
或者R 4、R 6与它们连接的碳原子一起形成任选取代(例如未取代的或者被氧代的)的C 5-C 6环烷基(例如形成
Figure PCTCN2022088560-appb-000127
)和5-6元杂环烷基，所述5-6元杂环烷基中的杂原子选自包含1、2、3或4个独立选自-NH、-O-、-S-和N的杂原子或杂原子团； Or R 4 , R 6 together with the carbon atom to which they are attached form an optionally substituted (eg unsubstituted or oxo) C 5 -C 6 cycloalkyl (eg forming
Figure PCTCN2022088560-appb-000127
) and a 5-6 membered heterocycloalkyl, the heteroatoms in the 5-6 membered heterocycloalkyl are selected from the group consisting of 1, 2, 3 or 4 independently selected from -NH, -O-, -S- and A heteroatom or heteroatom group of N;
R 7、R 8各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代。 R 7 and R 8 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace.
在一些实施方案中，所述S6中，当R 4、R 6与它们连接的碳原子一起形成任选取代的C 5-C 6环烷基和5-6元杂环烷基，所述取代是指被1、2、3或4个＝O取代。 In some embodiments, in the S6, when R 4 , R 6 and the carbon atom to which they are attached together form an optionally substituted C 5 -C 6 cycloalkyl and 5-6 membered heterocycloalkyl, the substituted means substituted with 1, 2, 3 or 4 =O.
在一些实施方案中，所述S6中，当R 4、R 6与它们连接的碳原子一起形成任选取代的5-6元杂环烷基时，S6中的
Figure PCTCN2022088560-appb-000128
片段为
Figure PCTCN2022088560-appb-000129
例如
Figure PCTCN2022088560-appb-000130
In some embodiments, in the S6, when R 4 , R 6 and the carbon atoms to which they are attached together form an optionally substituted 5-6 membered heterocycloalkyl, the
Figure PCTCN2022088560-appb-000128
Fragment is
Figure PCTCN2022088560-appb-000129
E.g
Figure PCTCN2022088560-appb-000130
在一些实施方案中，所述S6中，R 1为氢或-OR A，R A为氢。 In some embodiments, in the S6, R 1 is hydrogen or -OR A , and RA is hydrogen.
在一些实施方案中，所述S6中，R 1为氢。 In some embodiments, in the S6, R 1 is hydrogen.
在一些实施方案中，所述S6中，R 2为氢、C 1-C 4烷基、-O(C 1-C 4烷基)、-NH 2、-NH(C 1-C 4烷基)、-N(C 1-C 4烷基) 2或者卤素，所述C 1-C 4烷基和-O(C 1-C 4烷基)各自独立地任选被-O(C 1-C 4烷基)取代。 In some embodiments, in the S6, R 2 is hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl) ), -N(C 1 -C 4 alkyl) 2 or halogen, said C 1 -C 4 alkyl and -O(C 1 -C 4 alkyl) are each independently optionally -O(C 1 - C 4 alkyl) substituted.
在一些实施方案中，所述S6中，R 2为氢、C 1-C 4烷基、-O(C 1-C 4烷基)、-NH 2、-NH(C 1-C 4烷基)、-N(C 1-C 4烷基) 2或者卤素。 In some embodiments, in the S6, R 2 is hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl) ), -N(C 1 -C 4 alkyl) 2 or halogen.
在一些实施方案中，所述S6中，R 2为氢、C 1-C 4烷基或者-O(C 1-C 4烷基)，所述-O(C 1-C 4烷基)任选的被-O(C 1-C 4烷基)取代。 In some embodiments, in the S6, R 2 is hydrogen, C 1 -C 4 alkyl or -O(C 1 -C 4 alkyl), and -O(C 1 -C 4 alkyl) is any Optionally substituted with -O(C 1 -C 4 alkyl).
在另一些实施方案中，所述S6中，R 2为
Figure PCTCN2022088560-appb-000131
Figure PCTCN2022088560-appb-000132
In other embodiments, in said S6, R 2 is
Figure PCTCN2022088560-appb-000131
Figure PCTCN2022088560-appb-000132
在一些实施方案中，所述S6中，R 3为氢。 In some embodiments, in said S6, R3 is hydrogen.
在一些实施方案中，所述S6中，R 5为氢或者-NHR’。 In some embodiments, in the S6, R 5 is hydrogen or -NHR'.
在一些实施方案中，所述S6中，R 4为C 1-C 4卤代烷基；R 6为氢或者卤素；或者，R 4、R 6与它们连接的碳原子一起形成环使S6中的
Figure PCTCN2022088560-appb-000133
片段为
Figure PCTCN2022088560-appb-000134
In some embodiments, in the S6, R 4 is C 1 -C 4 haloalkyl; R 6 is hydrogen or halogen; or, R 4 , R 6 and the carbon atom to which they are attached together form a ring such that the
Figure PCTCN2022088560-appb-000133
Fragment is
Figure PCTCN2022088560-appb-000134
在一些实施方案中，所述S6中，R 7为C 1-C 6烷基。 In some embodiments, in the S6, R 7 is C 1 -C 6 alkyl.
在一些实施方案中，所述S6中，R 8为C 1-C 6烷基。 In some embodiments, in S6, R 8 is C 1 -C 6 alkyl.
在一些实施方案中，所述S6中，R 1为氢或-OR A； In some embodiments, in the S6, R 1 is hydrogen or -OR A ;
R A为氢； R A is hydrogen;
R 2为氢、C 1-C 4烷基或者-O(C 1-C 4烷基)(例如甲氧基)，所述-O(C 1-C 4烷基)任选的被-O(C 1-C 4烷基)(例如甲氧基)取代； R 2 is hydrogen, C 1 -C 4 alkyl, or -O(C 1 -C 4 alkyl) (eg, methoxy), optionally -O(C 1 -C 4 alkyl) (C 1 -C 4 alkyl) (eg methoxy) substituted;
R 3为氢； R 3 is hydrogen;
R 5为氢或者-NHR’； R 5 is hydrogen or -NHR';
R’选自氢、C 1-C 3烷基和-C(O)C 1-C 3烷基； R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
R 4为C 1-C 4卤代烷基； R 4 is C 1 -C 4 haloalkyl;
R 6为氢或者卤素； R 6 is hydrogen or halogen;
或者R 4、R 6与它们连接的碳原子一起形成环使S6中的
Figure PCTCN2022088560-appb-000135
片段为
Figure PCTCN2022088560-appb-000136
Or R 4 , R 6 and the carbon atoms to which they are attached together form a ring so that the
Figure PCTCN2022088560-appb-000135
Fragment is
Figure PCTCN2022088560-appb-000136
R 7为C 1-C 6烷基； R 7 is C 1 -C 6 alkyl;
R 8为C 1-C 6烷基。 R 8 is C 1 -C 6 alkyl.
在一些实施方案中，所述S6中，当R 2为C 1-C 4烷基时，所述C 1-C 4烷基可为甲基。 In some embodiments, in the S6, when R 2 is C 1 -C 4 alkyl, the C 1 -C 4 alkyl may be methyl.
在一些实施方案中，所述S6中，当R 2为-O(C 1-C 4烷基)时，所述-O(C 1-C 4烷基)可为-OCH 3。 In some embodiments, in the S6, when R 2 is -O(C 1 -C 4 alkyl), the -O(C 1 -C 4 alkyl) may be -OCH 3 .
在一些实施方案中，所述S6中，R 2为氢、甲基、-OCH 3或
Figure PCTCN2022088560-appb-000137
In some embodiments, in the S6, R 2 is hydrogen, methyl, -OCH 3 or
Figure PCTCN2022088560-appb-000137
在一些实施方案中，所述S6中，R 2为氢、甲基或-OCH 3。 In some embodiments, in S6, R 2 is hydrogen, methyl or -OCH 3 .
在一些实施方案中，所述S6中，R 3为氢。 In some embodiments, in said S6, R3 is hydrogen.
在一些实施方案中，所述S6中，当R’为C 1-C 3烷基时，所述C 1-C 3烷基可为乙基或异丙基。 In some embodiments, in the S6, when R' is a C 1 -C 3 alkyl group, the C 1 -C 3 alkyl group may be ethyl or isopropyl.
在一些实施方案中，所述S6中，当R’为-C(O)C 1-C 3烷基时，所述的-C(O)C 1-C 3烷基可为-C(O)CH 3。 In some embodiments, in the S6, when R' is -C(O)C 1 -C 3 alkyl, the -C(O)C 1 -C 3 alkyl can be -C(O ) CH 3 .
在一些实施方案中，所述S6中，R 5为氢或-NHR’，其中R’为氢、乙基、异丙基或-C(O)CH 3。 In some embodiments, in S6, R 5 is hydrogen or -NHR', wherein R' is hydrogen, ethyl, isopropyl or -C(O)CH 3 .
在一些优选的实施方案中，所述S6中，R 5为-NHR’，其中R’为氢。 In some preferred embodiments, in the S6, R 5 is -NHR', wherein R' is hydrogen.
在一些实施方案中，所述S6中，R 4为C 1-C 4卤代烷基； In some embodiments, in the S6, R 4 is C 1 -C 4 haloalkyl;
R 6为氢或者卤素； R 6 is hydrogen or halogen;
或者R 4、R 6与它们连接的碳原子一起形成环使S6中的
Figure PCTCN2022088560-appb-000138
片段为
Figure PCTCN2022088560-appb-000139
Or R 4 , R 6 and the carbon atoms to which they are attached together form a ring so that the
Figure PCTCN2022088560-appb-000138
Fragment is
Figure PCTCN2022088560-appb-000139
在一些实施方案中，所述S6中，当R 4为C 1-C 4卤代烷基时，所述的C 1-C 4卤代烷基可为C 1-C 4氟代烷 基，例如三氟甲基。 In some embodiments, in the S6, when R 4 is C 1 -C 4 haloalkyl, the C 1 -C 4 haloalkyl may be C 1 -C 4 fluoroalkyl, such as trifluoromethyl base.
在一些实施方案中，所述S6中，R 7为C 1-C 6烷基。 In some embodiments, in the S6, R 7 is C 1 -C 6 alkyl.
在一些实施方案中，所述S6中，当R 7为C 1-C 6烷基时，所述的C 1-C 6烷基可为甲基。 In some embodiments, in the S6, when R 7 is a C 1 -C 6 alkyl group, the C 1 -C 6 alkyl group may be a methyl group.
在一些实施方案中，所述S6中，R 8为C 1-C 6烷基。 In some embodiments, in S6, R 8 is C 1 -C 6 alkyl.
在一些实施方案中，所述S6中，当R 8为C 1-C 6烷基时，所述的C 1-C 6烷基可为甲基。 In some embodiments, in the S6, when R 8 is a C 1 -C 6 alkyl group, the C 1 -C 6 alkyl group may be a methyl group.
在一些实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000140
片段可为
Figure PCTCN2022088560-appb-000141
In some embodiments, the S6
Figure PCTCN2022088560-appb-000140
Fragments can be
Figure PCTCN2022088560-appb-000141
在一些实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000142
片段优选为
Figure PCTCN2022088560-appb-000143
In some embodiments, the S6
Figure PCTCN2022088560-appb-000142
Fragments are preferably
Figure PCTCN2022088560-appb-000143
在一些实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000144
片段优选为
Figure PCTCN2022088560-appb-000145
In some embodiments, the S6
Figure PCTCN2022088560-appb-000144
Fragments are preferably
Figure PCTCN2022088560-appb-000145
在一些实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000146
片段可为
Figure PCTCN2022088560-appb-000147
Figure PCTCN2022088560-appb-000148
优选为
Figure PCTCN2022088560-appb-000149
In some embodiments, the S6
Figure PCTCN2022088560-appb-000146
Fragments can be
Figure PCTCN2022088560-appb-000147
Figure PCTCN2022088560-appb-000148
preferably
Figure PCTCN2022088560-appb-000149
在一些优选的实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000150
片段为
Figure PCTCN2022088560-appb-000151
In some preferred embodiments, the S6
Figure PCTCN2022088560-appb-000150
Fragment is
Figure PCTCN2022088560-appb-000151
在一些更优选的实施方案中，所述S6中的
Figure PCTCN2022088560-appb-000152
片段为
Figure PCTCN2022088560-appb-000153
In some more preferred embodiments, the S6 in
Figure PCTCN2022088560-appb-000152
Fragment is
Figure PCTCN2022088560-appb-000153
优选的，本发明某些实施方式中，所述S6中R 8为甲基。 Preferably, in some embodiments of the present invention, R 8 in the S6 is methyl.
本发明某些实施方式中，所述S为S6'：In some embodiments of the present invention, the S is S6':
Figure PCTCN2022088560-appb-000154
Figure PCTCN2022088560-appb-000154
其中所述S6'中，R 2、R 3、R 4、R 5、R 6、R 7如S6中所定义和描述。 wherein in said S6', R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6.
本发明某些实施方式中，所述S6和S6'中，
Figure PCTCN2022088560-appb-000155
片段为
Figure PCTCN2022088560-appb-000156
In some embodiments of the present invention, in the S6 and S6',
Figure PCTCN2022088560-appb-000155
Fragment is
Figure PCTCN2022088560-appb-000156
本发明某些实施方式中，所述S为-X-S6'，S6'的结构如上所述；X为O、NH或S，优选为O。In some embodiments of the present invention, the S is -X-S6', and the structure of S6' is as described above; X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S6a：Preferably, in some embodiments of the present invention, the S is S6a:
Figure PCTCN2022088560-appb-000157
Figure PCTCN2022088560-appb-000157
其中所述S6a中，R 1、R 2、R 3、R 4、R 5、R 6、R 7如S6中所定义和描述。 wherein in said S6a, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S6或S6a中，R 1为氢；R 2选自-O(C 1-C 4烷基)；R 3为氢；R 4为C 1-C 4卤代烷基；R 5选自为-NH 2；R 7选自C 1-C 4烷基或C 1-C 4卤代烷基。 Preferably, in some embodiments of the present invention, in the S6 or S6a, R 1 is hydrogen; R 2 is selected from -O(C 1 -C 4 alkyl); R 3 is hydrogen; R 4 is C 1 - C 4 haloalkyl; R 5 is selected from -NH 2 ; R 7 is selected from C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.
优选的，本发明某些实施方式中，所述S为S6b：Preferably, in some embodiments of the present invention, the S is S6b:
Figure PCTCN2022088560-appb-000158
Figure PCTCN2022088560-appb-000158
其中所述S6b中，R 1、R 2、R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 wherein in said S6b, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为S6c：Preferably, in some embodiments of the present invention, the S is S6c:
Figure PCTCN2022088560-appb-000159
Figure PCTCN2022088560-appb-000159
其中所述S6c中，R 2、R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 wherein in said S6c, R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
本发明某些实施方式中，所述S为-X-S6c，S6c的结构和定义如上所述；其中，X为O、NH或者S，优选为O。In some embodiments of the present invention, the S is -X-S6c, and the structure and definition of S6c are as described above; wherein, X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S6d：Preferably, in some embodiments of the present invention, the S is S6d:
Figure PCTCN2022088560-appb-000160
Figure PCTCN2022088560-appb-000160
其中所述S6d中，X为O、NH或者S，优选为O；R 2、R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 Wherein in said S6d, X is O, NH or S, preferably O; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S6为WO2018115380A1(其全文通过引用的方式并入本文 中)中I-1至I-383的具体化合物。优选的，本发明某些实施方式中，所述S为S6e：Preferably, in certain embodiments of the present invention, the S6 is a specific compound of I-1 to I-383 in WO2018115380A1 (the entirety of which is incorporated herein by reference). Preferably, in some embodiments of the present invention, the S is S6e:
Figure PCTCN2022088560-appb-000161
Figure PCTCN2022088560-appb-000161
其中所述S6e中，R 2、R 3和R 7如S6的任一方案中所定义和描述。 wherein in said S6e, R 2 , R 3 and R 7 are as defined and described in any one of the schemes of S6.
优选的，本发明某些实施方式中，所述S为-X-S6e，S6e的结构和定义如上所述；其中，X为O、NH或者S，优选为O。Preferably, in some embodiments of the present invention, the S is -X-S6e, and the structure and definition of S6e are as described above; wherein, X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S6e中，R 2为-O(C 1-C 4烷基)；R 3为氢；R 7为C 1-C 6烷基。 Preferably, in some embodiments of the present invention, in the S6e, R 2 is -O(C 1 -C 4 alkyl); R 3 is hydrogen; R 7 is C 1 -C 6 alkyl.
优选的，本发明某些实施方式中，所述S6e中，R 2为-OCH 3；R 3为氢；R 7为甲基。 Preferably, in some embodiments of the present invention, in the S6e, R 2 is -OCH 3 ; R 3 is hydrogen; R 7 is methyl.
本发明某些实施方式中，所述S6、S6'、S6a或S6c为如下任一结构：In some embodiments of the present invention, the S6, S6', S6a or S6c is any of the following structures:
Figure PCTCN2022088560-appb-000162
Figure PCTCN2022088560-appb-000162
优选的，本发明某些实施方式中，所述S6、S6'、S6a或S6c为
Figure PCTCN2022088560-appb-000163
Preferably, in some embodiments of the present invention, the S6, S6', S6a or S6c is
Figure PCTCN2022088560-appb-000163
优选的，本发明某些实施方式中，所述S6、S6'、S6a、S6c或S6e为
Figure PCTCN2022088560-appb-000164
Preferably, in some embodiments of the present invention, the S6, S6', S6a, S6c or S6e are
Figure PCTCN2022088560-appb-000164
本发明某些实施方式中，所述S为
Figure PCTCN2022088560-appb-000165
In some embodiments of the present invention, the S is
Figure PCTCN2022088560-appb-000165
本发明某些实施方式中，所述S为S6”:In some embodiments of the present invention, described S is S6 ":
Figure PCTCN2022088560-appb-000166
Figure PCTCN2022088560-appb-000166
其中所述S6”中，R 1、R 3、R 4、R 5、R 6、R 7和R 8如S6中所定义和描述。 wherein in said S6", R 1 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined and described in S6.
本发明某些实施方式中，所述S为S6”':In some embodiments of the present invention, described S is S6 "':
Figure PCTCN2022088560-appb-000167
Figure PCTCN2022088560-appb-000167
其中所述S6”'中，R 3、R 4、R 5、R 6、R 7和R 8如S6中所定义和描述。 wherein in said S6"', R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined and described in S6.
本发明某些实施方式中，所述S6”和S6”'中，
Figure PCTCN2022088560-appb-000168
片段为
Figure PCTCN2022088560-appb-000169
In some embodiments of the present invention, in the S6" and S6"',
Figure PCTCN2022088560-appb-000168
Fragment is
Figure PCTCN2022088560-appb-000169
本发明某些实施方式中，所述S为-X-S6”'，S6”'的结构如上所述；其中X为O、NH或S，优选为O。In some embodiments of the present invention, the S is -X-S6"', and the structure of S6"' is as described above; wherein X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S6”为
Figure PCTCN2022088560-appb-000170
Preferably, in some embodiments of the present invention, the S6" is
Figure PCTCN2022088560-appb-000170
优选的，本发明某些实施方式中，所述S为S6a”：Preferably, in some embodiments of the present invention, the S is S6a":
Figure PCTCN2022088560-appb-000171
Figure PCTCN2022088560-appb-000171
其中所述S6a”中，R 1、R 3、R 4、R 5、R 6、R 7如S6中所定义和描述。 wherein in said S6a", R 1 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为S6b”：Preferably, in some embodiments of the present invention, the S is S6b":
Figure PCTCN2022088560-appb-000172
Figure PCTCN2022088560-appb-000172
其中所述S6b”中，R 1、R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 wherein in said S6b", R 1 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为S6c”：Preferably, in some embodiments of the present invention, the S is S6c":
Figure PCTCN2022088560-appb-000173
Figure PCTCN2022088560-appb-000173
其中所述S6c”中，R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 wherein in said S6c", R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为-X-S6c”，S6c”的结构和定义如上所述；其中，X为O、NH或者S，优选为O。Preferably, in some embodiments of the present invention, the S is -X-S6c", and the structure and definition of S6c" are as described above; wherein, X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S为S6d”：Preferably, in some embodiments of the present invention, the S is S6d":
Figure PCTCN2022088560-appb-000174
Figure PCTCN2022088560-appb-000174
其中所述S6d”中，X为O、NH或者S，优选为O；R 3、R 4、R 5、R 6和R 7如S6中所定义和描述。 Wherein said S6d", X is O, NH or S, preferably O; R 3 , R 4 , R 5 , R 6 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为S6e”：Preferably, in some embodiments of the present invention, the S is S6e":
Figure PCTCN2022088560-appb-000175
Figure PCTCN2022088560-appb-000175
其中所述S6e”中，R 3和R 7如S6中所定义和描述。 wherein said S6e", R 3 and R 7 are as defined and described in S6.
优选的，本发明某些实施方式中，所述S为-X-S6e”，S6e”的结构和定义如上所述；其中，X为O、NH或者S，优选为O。Preferably, in some embodiments of the present invention, the S is -X-S6e", and the structure and definition of S6e" are as described above; wherein, X is O, NH or S, preferably O.
优选的，本发明某些实施方式中，所述S6e”中，R 3为氢；R 7为C 1-C 6烷基。 Preferably, in some embodiments of the present invention, in the S6e", R 3 is hydrogen; R 7 is C 1 -C 6 alkyl.
优选的，本发明某些实施方式中，所述S6e”中，R 3为氢；R 7为甲基。 Preferably, in some embodiments of the present invention, in the S6e", R 3 is hydrogen; R 7 is methyl.
优选的，本发明某些实施方式中，所述S6”、S6”'、S6a”、S6c”或S6e”为
Figure PCTCN2022088560-appb-000176
Preferably, in some embodiments of the present invention, the S6", S6"', S6a", S6c" or S6e" are
Figure PCTCN2022088560-appb-000176
优选的，本发明某些实施方式中，所述S为Preferably, in some embodiments of the present invention, the S is
Figure PCTCN2022088560-appb-000177
Figure PCTCN2022088560-appb-000177
更优选的，本发明某些实施方式中，所述S为More preferably, in some embodiments of the present invention, the S is
Figure PCTCN2022088560-appb-000178
或者
Figure PCTCN2022088560-appb-000179
Figure PCTCN2022088560-appb-000178
or
Figure PCTCN2022088560-appb-000179
更优选的，本发明某些实施方式中，所述S为
Figure PCTCN2022088560-appb-000180
More preferably, in some embodiments of the present invention, the S is
Figure PCTCN2022088560-appb-000180
本发明某些实施方式中，L为键。In certain embodiments of the present invention, L is a bond.
本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个或多个亚甲基任选的被选自-NR 3’-、-O-、-S-、-S(O)-、-S(O)NR 3’-、-NR 3’S(O)-、-S(O) 2-、-S(O) 2NR 3’-、-NR 3’S(O) 2-、-NR 4’S(O) 2NR 3’-、-CR 1’R 2’-、-C(O)-、-C(O)O-、-OC(O)-、-NR 3’C(O)O-、-OC(O)NR 3’-、-C(O)NR 3’-、-NR 3’C(O)-、-NR 4’C(O)NR 3’-、-P(O)-、 -P(O)O-、-OP(O)-、-OP(O)O-、亚乙烯基、亚乙炔基、3-12元亚环烷基、含有1个或多个选自N、O或S杂原子的3-12元亚杂环烷基、6-10元亚芳基或5-10元亚杂芳基的基团替代，所述亚乙烯基、亚环烷基、亚杂环烷基、亚芳基、亚杂芳基各自独立的任选的被1个或多个选自卤素、-OR 3’、-NR 3’R 4’、氧代、硝基、氰基、C1-C6烷基、-S(C1-C6烷基)、C3-C10环烷基、C3-C10杂环烷基、6-10芳基、5-10元杂芳基、-C(O)R 1’、-C(O)OR 3’、-OC(O)R 1’、-C(O)NR 3’、-NR 3’C(O)R 1’、-S(O)R 1’、-S(O)NR 3’、-S(O) 2R 1’、-S(O) 2NR 3’、-NR 3’S(O) 2R 1’、-NR 4’S(O) 2NR 3’、-OC(O)NR 3’、-NR 4’C(O)NR 3’的取代基取代，所述烷基、环烷基、杂环烷基、芳基、杂芳基各自独立的任选的被1个或多个选自卤素、-OH、-NR 3’R 4’、氧代、硝基、氰基、C 1-C 6烷基、C 3-C 10环烷基、C 3-C 10杂环烷基、6-10元芳基、5-10元杂芳基的取代基取代；R 1’、R 2’各自独立为卤素、-OH、-NR 3’R 4’、C 1-C 6烷基、氯代C 1-C 6烷基、羟基C 1-C 6烷基、-O(C 1-C 6烷基)、-NH(C 1-C 6烷基)、-NH(C 1-C 6烷基)2、C 3-C 10环烷基、-O(C 3-C 10环烷基)、-NH(C 3-C 10环烷基)、C 3-C 10杂环烷基、-O(C 3-C 10杂环烷基)、-NH(C 3-C 10杂环烷基)、6-10元芳基、-O(6-10元芳基)、-NH(6-10元芳基)、5-10元杂芳基、-O(5-10元杂芳基)、-NH(5-10元杂芳基)，R 3’、R 4’各自独立的为氢、氘、C 1-C 6烷基、C 3-C 10环烷基、C 3-C 10杂环烷基、6-10元芳基、5-10元杂芳基；j为1、2、3、4、5、6、7、8、9、10、11、12、13、14、15、16、17、18、19、20、21、22、23、24或25。 In certain embodiments of the present invention, L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, - O-, -S-, -S(O)-, -S(O)NR 3' -, -NR 3' S(O)-, -S(O) 2 -, -S(O) 2 NR 3 ' -, -NR 3' S(O) 2 -, -NR 4' S(O) 2 NR 3' -, -CR 1' R 2' -, -C(O)-, -C(O)O -, -OC(O)-, -NR 3' C(O)O-, -OC(O)NR 3' -, -C(O)NR 3' -, -NR 3' C(O)-, -NR 4' C(O)NR 3' -, -P(O)-, -P(O)O-, -OP(O)-, -OP(O)O-, vinylidene, ethynylene , 3-12-membered cycloalkylene, 3-12-membered heterocycloalkylene containing 1 or more heteroatoms selected from N, O or S, 6-10-membered arylene or 5-10-membered heteroatom Aryl group replacement, the vinylidene, cycloalkylene, heterocycloalkylene, arylene, heteroarylene are each independently optional by 1 or more selected from halogen, -OR 3' , -NR 3' R 4' , oxo, nitro, cyano, C1-C6 alkyl, -S(C1-C6 alkyl), C3-C10 cycloalkyl, C3-C10 heterocycloalkyl , 6-10 aryl, 5-10 membered heteroaryl, -C(O)R 1' , -C(O)OR 3' , -OC(O)R 1' , -C(O)NR 3' , -NR 3' C(O)R 1' , -S(O)R 1' , -S(O)NR 3' , -S(O) 2 R 1' , -S(O) 2 NR 3' Substituents of , -NR 3' S(O) 2 R 1' , -NR 4' S(O) 2 NR 3' , -OC(O)NR 3' , -NR 4' C(O)NR 3' Substituted, the alkyl group, cycloalkyl group, heterocycloalkyl group, aryl group, and heteroaryl group are each independently optionally substituted by one or more selected from halogen, -OH, -NR 3' R 4' , oxygen substituted, nitro, cyano, C 1 -C 6 alkyl, C 3 -C 10 cycloalkyl, C 3 -C 10 heterocycloalkyl, 6-10-membered aryl, 5-10-membered heteroaryl Substituent substitution; R 1' , R 2' are each independently halogen, -OH, -NR 3' R 4' , C 1 -C 6 alkyl, chloro C 1 -C 6 alkyl, hydroxy C 1 -C 6 alkyl, -O(C 1 -C 6 alkyl), -NH(C 1 -C 6 alkyl), -NH(C 1 -C 6 alkyl) 2, C 3 -C 10 cycloalkyl, -O(C 3 -C 10 cycloalkyl), -NH(C 3 -C 10 cycloalkyl), C 3 -C 10 heterocycloalkyl, -O(C 3 -C 10 heterocycloalkyl), -NH(C 3 -C 10 heterocycloalkyl), 6-10 membered aryl, -O(6-10 membered aryl), -NH(6-10 membered aryl), 5-10 membered heteroaryl, -O(5-10 membered heteroaryl), -NH(5-10 membered heteroaryl) Aryl), R 3' and R 4' are each independently hydrogen, deuterium, C 1 -C 6 alkyl, C 3 -C 10 cycloalkyl, C 3 -C 10 heterocycloalkyl, 6-10 membered Aryl, 5-10 membered heteroaryl; j is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 , 20, 21, 22, 23, 24 or 25.
优选的，本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个或多个亚甲基任选的被选自-NR 3’-、-O-、-CR 1’R 2’-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NR 3’-、-NR 3’C(O)-、-S(O) 2NR 3’-、-NR 3’S(O) 2-、亚乙烯基、亚乙炔基、苯基、8-10元双环亚芳基、3-7元饱和或部分不饱和的亚环烷基、5-11元的饱和或部分不饱和的亚螺环烷基、5-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮、氧或硫杂原子的4-7元饱和或部分不饱和的亚杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的5-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的5-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮、氧或硫杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基、具有1-4个独立地选自氮、氧或硫杂原子的5-6元亚杂芳基、或具有1-5个选自氮、氧或硫杂原子的8-10元双环杂芳基的基团替代，所述亚乙烯基、亚乙炔基、亚环烷基、亚杂环烷基、苯基、亚螺杂环烷基、亚稠杂环烷基、亚螺环烷基、亚稠环烷基、亚杂芳基各自独立的任选的被1个或多个选自卤素、氧代、-NR 3’R 4’、-OR 3’、硝基、-CN、C 1-C 6烷基、C 3-C 10环烷基、C 3-C 10杂环烷基的取代基取代，所述烷基、环烷基、杂环烷基任选被1个或多个选自卤素、-OH、-NH 2、-CN、C 1-C 4烷基、C 3-C 6环烷基的取代基取代，R 1’、R 2’各自独立为卤素、-OH、-NH 2、C 1-C 4烷基、C 1-C 4氯代烷基、C 1-C 4羟基烷基、-O(C 1-C 4烷基)、-NH(C 1-C 4烷基)、-NH(C 1-C 4烷基)、C 3-C 6环烷基、-O(C 3-C 6环烷基)、-NH(C 3-C 6环烷基)、C 3-C 6杂环烷基、-O(C 3-C 6杂环烷基)、-NH(C 3-C 6环烷基)；R 3’、R 4’各自独立的为氢、氘、C 1-C 4烷基、C 3-C 6环烷基、C 3-C 6杂环烷基，j为2、3、4、5、6、7、8、9、10、11或12。 Preferably, in certain embodiments of the present invention, L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, -O-, -CR 1' R 2' -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O) -, -C(O)NR 3' -, -NR 3' C(O)-, -S(O) 2 NR 3' -, -NR 3' S(O) 2 -, vinylidene, acetylene base, phenyl, 8-10 membered bicyclic arylene, 3-7 membered saturated or partially unsaturated cycloalkylene, 5-11 membered saturated or partially unsaturated spirocycloalkylene, 5-11 membered Saturated or partially unsaturated fused cycloalkylene, 8-10 membered bicyclic saturated or partially unsaturated cycloalkylene, 4-7 membered with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur Saturated or partially unsaturated heterocycloalkylene, 5-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur, with 1-2 5-11 membered saturated or partially unsaturated fused heterocycloalkylene independently selected from nitrogen, oxygen or sulfur heteroatoms, 8-10 members with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur heteroatoms membered bicyclic saturated or partially unsaturated heterocycloalkylene, 5-6 membered heteroarylene having 1-4 heteroatoms independently selected from nitrogen, oxygen or sulfur, or having 1-5 heteroatoms selected from nitrogen, 8-10 membered bicyclic heteroaryl radical substitution of oxygen or sulfur heteroatoms, the vinylene, ethynylene, cycloalkylene, heterocycloalkylene, phenyl, spiroheterocycloalkylene, Condensed heterocycloalkylene, spirocycloalkylene, condensed cycloalkylene, and heteroarylene are each independently optional by one or more selected from halogen, oxo, -NR 3' R 4' , Substituents of -OR 3' , nitro, -CN, C 1 -C 6 alkyl, C 3 -C 10 cycloalkyl, C 3 -C 10 heterocycloalkyl, said alkyl, cycloalkyl , Heterocycloalkyl is optionally substituted by one or more substituents selected from halogen, -OH, -NH 2 , -CN, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, R 1 ' and R 2' are each independently halogen, -OH, -NH 2 , C 1 -C 4 alkyl, C 1 -C 4 chloroalkyl, C 1 -C 4 hydroxyalkyl, -O(C 1 - C 4 alkyl), -NH (C 1 -C 4 alkyl), -NH (C 1 -C 4 alkyl), C 3 -C 6 cycloalkyl, -O(C 3 -C 6 cycloalkyl) ), -NH(C 3 -C 6 cycloalkyl), C 3 -C 6 heterocycloalkyl, -O(C 3 -C 6 heterocycloalkyl), -NH(C 3 -C 6 cycloalkyl) ); R 3' and R 4' are each independently hydrogen, deuterium, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 heterocycloalkyl, and j is 2 , 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12.
优选的，本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个或多个亚甲基任选的被选自-NR 3’-、-O-、-CR 1’R 2’-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NR 3’-、-NR 3’C(O)-、-S(O) 2NR 3’-、-NR 3’S(O) 2-、亚乙烯基、亚乙炔基、苯基、8-10元双环亚芳基、3-7元饱和或部分不饱和的单环亚环烷基、5-11元的饱和或部分不饱和的亚螺环烷基、5-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮或氧杂原子的5-7元饱和或部分不饱和的亚杂环烷基、具有1-2个独立的选自氮或氧杂原子的5-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮或氧杂原子的5-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮或氧杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基、具有1-4个独立地选自氮或氧杂原子的5-6元亚杂芳基、或具有1-5个选自氮或氧杂原子的8-10元双环杂芳基的基团替代，所述亚乙烯基、亚乙炔基、亚环烷基、亚杂环烷基、苯基、亚螺杂环烷基、亚稠杂环烷基、亚稠环烷基、亚螺环烷基、亚杂芳基各自独立的任选的被1个或多个选自卤素、氧代、-NR 3’R 4’、-OR 3’、硝基、-CN、C 1-C 6烷基、C 3-C 6环烷基、C 3-C 6杂环烷基的取代基取代，所述烷基、环烷基、杂环烷基任选被1个或多个选自卤素、-OH、-NH2、-CN、C1-C4烷基、C3-C6环烷基的取代基取代，R 1’、R 2’各自独立为卤素、-OH、-NH 2、C 1-C 4烷基、C 1-C 4氯代烷基、C 1-C 4羟基烷基、-O(C 1-C 4烷基)、-NH(C 1-C 4烷基)、-NH(C 1-C 4烷基)、C 3-C 6环烷基、-O(C 3-C 6环烷基)、-NH(C 3-C 6环烷基)、C 3-C 6杂环烷基、-O(C 3-C 6杂环烷基)、-NH(C 3-C 6环烷基)；R 3’、R 4’各自独立的为氢、氘、C 1-C 4烷基、C 3-C 6环烷基、C 3-C 6杂环烷基，j为2、3、4、5、6、7、8、9或10。 Preferably, in certain embodiments of the present invention, L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally selected from -NR 3' -, -O-, -CR 1' R 2' -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O) -, -C(O)NR 3' -, -NR 3' C(O)-, -S(O) 2 NR 3' -, -NR 3' S(O) 2 -, vinylidene, acetylene base, phenyl, 8-10 membered bicyclic arylene, 3-7 membered saturated or partially unsaturated monocyclic cycloalkylene, 5-11 membered saturated or partially unsaturated spirocycloalkylene, 5- 11-membered saturated or partially unsaturated fused cycloalkylene, 8-10 membered bicyclic saturated or partially unsaturated cycloalkylene, 5-7 membered with 1-2 heteroatoms independently selected from nitrogen or oxygen Saturated or partially unsaturated heterocycloalkylene, 5-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen or oxygen, with 1-2 independent 5-11-membered saturated or partially unsaturated fused heterocycloalkylidene selected from nitrogen or oxygen heteroatoms, 8-10-membered bicyclic saturated or partially unsaturated heteroatoms with 1-2 heteroatoms independently selected from nitrogen or oxygen Saturated heterocycloalkylene, 5-6 membered heteroarylene with 1-4 heteroatoms independently selected from nitrogen or oxygen, or 8-10 membered with 1-5 heteroatoms selected from nitrogen or oxygen Group substitution of bicyclic heteroaryl, the vinylene, ethynylene, cycloalkylene, heterocycloalkylene, phenyl, spiroheterocycloalkylene, fused heterocycloalkylene, fused ring Alkyl, spirocycloalkylene, heteroarylene are each independently optionally selected from halogen, oxo, -NR 3' R 4' , -OR 3' , nitro, -CN , C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 heterocycloalkyl substituents, the alkyl, cycloalkyl and heterocycloalkyl are optionally substituted by one or multiple substituents selected from halogen, -OH, -NH2, -CN, C1-C4 alkyl, C3-C6 cycloalkyl, R 1' , R 2' are each independently halogen, -OH, -NH 2 , C 1 -C 4 alkyl, C 1 -C 4 chloroalkyl, C 1 -C 4 hydroxyalkyl, -O(C 1 -C 4 alkyl), -NH(C 1 -C 4 alkane base), -NH(C 1 -C 4 alkyl), C 3 -C 6 cycloalkyl, -O(C 3 -C 6 cycloalkyl), -NH(C 3 -C 6 cycloalkyl), C 3 -C 6 heterocycloalkyl, -O(C 3 -C 6 heterocycloalkyl), -NH(C 3 -C 6 cycloalkyl); R 3' and R 4' are each independently hydrogen, Deuterium, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 heterocycloalkyl, j is 2, 3, 4, 5, 6, 7, 8, 9 or 10.
优选的，本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个、2个、3个、4个或者5个亚甲基任选的被选自-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-CHF-、-CHCF 3-、-C(O)-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-、-NCH 3C(O)-、亚乙烯基、亚乙炔基、亚环丙基、亚环丁基、亚环戊基、亚环己基、亚氧杂环丙基、亚氧杂环丁基、亚氧杂环戊基、亚氧杂环己基、亚氮杂环丙基、亚氮杂环丁基、亚氮杂环戊基、亚哌啶基、亚哌嗪基、亚吗啉基、亚高吗啉基、亚苯基、亚吡咯基、亚噻吩基、亚呋喃基、亚咪唑基、亚吡唑基、亚三唑基、亚四唑基、亚噁唑基、亚异噁唑基、亚噻唑基、亚异噻唑基、亚吡啶基、亚嘧啶基、亚哒嗪基、亚吡嗪基、
Figure PCTCN2022088560-appb-000181
Figure PCTCN2022088560-appb-000182
的基团替代，且所述替代基团任选的被1个或多个选自卤素、氧代、-NR 3’R 4’、-OR 3’、C1-C4烷基的取代基取代，所述烷基任选被1个或多个选自卤素、-OH、-NH 2的取代基取代，R 3’、R 4’各自独立的为氢、氘、C1-C4烷基，j为2、3、4、5、6、7、8、9或者10。 Preferably, in some embodiments of the present invention, L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from the group consisting of -NH-, -NCH3-, -O-, -C( CH3 ) 2- , -CHF-, -CHCF3- , -C(O)-, -C(O)O- , -OC(O)-, -C(O)NH-, -C(O)NCH 3 -, -NHC(O)-, -NCH 3 C(O)-, vinylidene, ethynylene, Cyclopropyl, cyclobutylene, cyclopentylene, cyclohexylene, oxiranylene, oxetylene, oxolane, oxane, aziridine base, azetidine, azetidine, piperidinylene, piperazinylene, morpholinylene, homomorpholinylene, phenylene, pyrrolidene, thienylene, thienylene Furyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyridylene, pyrimidinylene, Pyridazinylene, Pyrazinylene,
Figure PCTCN2022088560-appb-000181
Figure PCTCN2022088560-appb-000182
and the substitution group is optionally substituted by one or more substituents selected from halogen, oxo, -NR 3' R 4' , -OR 3' , C1-C4 alkyl, The alkyl is optionally substituted by one or more substituents selected from halogen, -OH, -NH 2 , R 3' and R 4' are each independently hydrogen, deuterium, C1-C4 alkyl, and j is 2, 3, 4, 5, 6, 7, 8, 9 or 10.
优选的，本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个、2个、3个、4个或者5个亚甲基任选的被选自-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-CHF-、-CHCF 3-、-C(O)-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-、-NCH 3C(O)-、亚环丙基、亚环丁基、亚环戊基、亚环己基、亚氧杂环丙基、亚氧杂环丁基、亚氧杂环戊基、亚氧杂环己基、亚氮杂环丙基、亚氮杂环丁基、亚氮杂环戊基、亚哌啶基、亚哌嗪基、亚吗啉基、亚高吗啉基、
Figure PCTCN2022088560-appb-000183
Figure PCTCN2022088560-appb-000184
的基团替代，且所述替代基团任选的被1个或多个选自F、Cl、氧代、-NR 3’R 4’、-OR 3’、C 1-C 4烷基的取代基取代，所述烷基任选被1个或多个选自卤素、-OH、-NH 2的取代基取代，R 3’、R 4’各自独立的为氢、氘、甲基、乙基、丙基，j为3、4、5、6、7、8、9或者10。 Preferably, in some embodiments of the present invention, L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from the group consisting of -NH-, -NCH3-, -O-, -C( CH3 ) 2- , -CHF-, -CHCF3- , -C(O)-, -C(O)O- , -OC(O)-, -C(O)NH-, -C(O)NCH 3 -, -NHC(O)-, -NCH 3 C(O)-, cyclopropylene, cyclobutylene , cyclopentylene, cyclohexylene, oxane, oxetylene, oxolane, oxane, aziridine, aziridine , nitrosyl, piperidinide, piperazinide, morpholinide, homomorpholinide,
Figure PCTCN2022088560-appb-000183
Figure PCTCN2022088560-appb-000184
and the substitution group is optionally replaced by 1 or more selected from F, Cl, oxo, -NR 3' R 4' , -OR 3' , C 1 -C 4 alkyl Substituents are substituted, the alkyl is optionally substituted by one or more substituents selected from halogen, -OH, -NH 2 , R 3' , R 4' are each independently hydrogen, deuterium, methyl, ethyl group, propyl group, j is 3, 4, 5, 6, 7, 8, 9 or 10.
优选的，本发明某些实施方式中，L为-(CH 2) j-，所述-(CH 2) j-中的1个、2个、3个、4个或者5个亚甲基任选的被选自-O-、-NH-、-NCH 3-、-C(O)-、-C(O)NH-、-NHC(O)-、-NCH 3C(O)-、-C(O)NCH 3-、亚环己基、亚氮杂环丙基、亚氮杂环丁基、亚氮杂环戊基、亚哌啶基、亚哌嗪基、
Figure PCTCN2022088560-appb-000185
Figure PCTCN2022088560-appb-000186
的基团替代，j为4、5、6、7、8、9或者10。 Preferably, in some embodiments of the present invention, L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are any selected from -O-, -NH-, -NCH3-, -C(O)-, -C(O)NH-, -NHC(O) - , -NCH3C (O)-, - C(O)NCH 3 -, cyclohexylene, azidopropyl, azidobutyl, azidopentyl, piperidinylene, piperazinylene,
Figure PCTCN2022088560-appb-000185
Figure PCTCN2022088560-appb-000186
group substitution, j is 4, 5, 6, 7, 8, 9 or 10.
优选的，本发明某些实施方式中，L选自-(CH 2) j-1-C(O)-，所述-(CH 2) j-1-C(O)-中的亚甲基如上述L中所定义，任选被1个或多个基团所替代，所述j如上述L中所定义。 Preferably, in certain embodiments of the present invention, L is selected from -(CH 2 ) j-1 -C(O)-, the methylene group in the -(CH 2 ) j-1 -C(O)- as defined in L above, optionally substituted by one or more groups, and said j is as defined in L above.
优选的，本发明某些实施方式中，L选自Preferably, in some embodiments of the present invention, L is selected from
Figure PCTCN2022088560-appb-000187
Figure PCTCN2022088560-appb-000187
Figure PCTCN2022088560-appb-000188
Figure PCTCN2022088560-appb-000188
Figure PCTCN2022088560-appb-000189
Figure PCTCN2022088560-appb-000189
Figure PCTCN2022088560-appb-000190
Figure PCTCN2022088560-appb-000190
Figure PCTCN2022088560-appb-000191
Figure PCTCN2022088560-appb-000191
Figure PCTCN2022088560-appb-000192
Figure PCTCN2022088560-appb-000192
Figure PCTCN2022088560-appb-000193
Figure PCTCN2022088560-appb-000193
Figure PCTCN2022088560-appb-000194
Figure PCTCN2022088560-appb-000194
Figure PCTCN2022088560-appb-000195
Figure PCTCN2022088560-appb-000195
Figure PCTCN2022088560-appb-000196
Figure PCTCN2022088560-appb-000196
Figure PCTCN2022088560-appb-000197
Figure PCTCN2022088560-appb-000197
Figure PCTCN2022088560-appb-000198
Figure PCTCN2022088560-appb-000198
Figure PCTCN2022088560-appb-000199
Figure PCTCN2022088560-appb-000199
Figure PCTCN2022088560-appb-000200
Figure PCTCN2022088560-appb-000200
Figure PCTCN2022088560-appb-000201
Figure PCTCN2022088560-appb-000201
Figure PCTCN2022088560-appb-000202
Figure PCTCN2022088560-appb-000202
Figure PCTCN2022088560-appb-000203
Figure PCTCN2022088560-appb-000203
Figure PCTCN2022088560-appb-000204
Figure PCTCN2022088560-appb-000204
Figure PCTCN2022088560-appb-000205
Figure PCTCN2022088560-appb-000205
Figure PCTCN2022088560-appb-000206
Figure PCTCN2022088560-appb-000206
Figure PCTCN2022088560-appb-000207
Figure PCTCN2022088560-appb-000207
Figure PCTCN2022088560-appb-000208
Figure PCTCN2022088560-appb-000208
Figure PCTCN2022088560-appb-000209
Figure PCTCN2022088560-appb-000209
Figure PCTCN2022088560-appb-000210
Figure PCTCN2022088560-appb-000210
Figure PCTCN2022088560-appb-000211
Figure PCTCN2022088560-appb-000211
本发明某些实施方式中，所述L为如下任一结构：In some embodiments of the present invention, the L is any of the following structures:
Figure PCTCN2022088560-appb-000212
Figure PCTCN2022088560-appb-000212
Figure PCTCN2022088560-appb-000213
Figure PCTCN2022088560-appb-000213
优选的，本发明某些实施方式中，所述L为LA，Preferably, in some embodiments of the present invention, the L is LA,
Figure PCTCN2022088560-appb-000214
Figure PCTCN2022088560-appb-000214
其中所述LA中：Where said LA:
环A为键、C 3-C 12亚环烷基(例如
Figure PCTCN2022088560-appb-000215
其中a端与S连接，b端与X”'连接)或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基(例如
Figure PCTCN2022088560-appb-000216
Figure PCTCN2022088560-appb-000217
其中a端与S连接，b端与X”'连接)，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring A is a bond, C 3 -C 12 cycloalkylene (eg
Figure PCTCN2022088560-appb-000215
wherein the a-terminus is attached to S and the b-terminus is attached to X"') or a 3-12 membered heterocycloalkylene group containing 1-2 heteroatoms selected from N, O or S (e.g.
Figure PCTCN2022088560-appb-000216
Figure PCTCN2022088560-appb-000217
wherein the a terminal is attached to S and the b terminal is attached to X"'), the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxy, C 1 -C 6 Substituent substitution of alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
环B为键、C 3-C 12亚环烷基(例如，
Figure PCTCN2022088560-appb-000218
其中c端与X”'连接，d端与L 3连接)或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基(例如
Figure PCTCN2022088560-appb-000219
Figure PCTCN2022088560-appb-000220
其中c端与X”'连接，d端与L 3连接)，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring B is a bond, C 3 -C 12 cycloalkylene (eg,
Figure PCTCN2022088560-appb-000218
wherein the c-terminus is attached to X"' and the d-terminus is attached to L3) or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S (eg
Figure PCTCN2022088560-appb-000219
Figure PCTCN2022088560-appb-000220
wherein the c-terminus is attached to X"' and the d - terminus is attached to L3), the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxyl, C1 -C Substituent substitution of 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
环C为C 3-C 12亚环烷基(例如
Figure PCTCN2022088560-appb-000221
其中e端与L 3连接，f端与X”连接)或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基(例如
Figure PCTCN2022088560-appb-000222
Figure PCTCN2022088560-appb-000223
其中e端与L 3连接，f端与X”连接)，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring C is C 3 -C 12 cycloalkylene (eg
Figure PCTCN2022088560-appb-000221
wherein the e-terminus is attached to L and the f-terminus is attached to X") or a 3-12 membered heterocycloalkylene group containing 1-2 heteroatoms selected from N, O or S (e.g.
Figure PCTCN2022088560-appb-000222
Figure PCTCN2022088560-appb-000223
wherein the e-terminus is attached to L and the f - terminus is attached to X"), the cycloalkylene and heterocycloalkylene are optionally selected from halogen, oxo, cyano, amino, hydroxyl, C1 - C6 Substituent substitution of alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl or -O-(C 1 -C 6 alkyl);
X”为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-、-NCH 3C(O)-或-C(O)CH 2O-； X" is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C( O) NCH3- , -NHC(O)-, -NCH3C (O)- or -C(O) CH2O- ;
L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被选自-O-、-NH-、-C≡C-、-N(C 1-C 6烷基)-、-N(C 1-C 6卤代烷基)-、-C(O)-、-N(C 1-C 6羟基烷基)-或-N(C 3-C 8环烷基)-替代，k为0、1、2、3、4、5、6或7； L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally selected from -O-, -NH-, -C≡C-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -C(O)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 -C 8 cycloalkane base)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
X”'为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-CH 2NCH 3-、-NHC(O)-或-NCH 3C(O)-。 X"' is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C (O) NCH3- , -CH2NCH3- , -NHC(O) - or -NCH3C (O)-.
在一些实施方案中，所述LA中：In some embodiments, in the LA:
环A为键、C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring A is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
环B为键、C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基 和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring B is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
环C为C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring C is C 3 -C 12 cycloalkylene or 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, said cycloalkylene and heterocycloalkylene is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 -C 6 alkyl) substituent substitution;
X”为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-或-NCH 3C(O)-； X" is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C( O) NCH 3 -, -NHC(O)- or -NCH 3 C(O)-;
L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被选自-O-、-NH-、-N(C 1-C 6烷基)-、-N(C 1-C 6卤代烷基)-、-N(C 1-C 6羟基烷基)-或-N(C 3-C 8环烷基)-替代，k为0、1、2、3或4； L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally selected from -O-, -NH-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 -C 8 cycloalkyl)- substitution, k is 0, 1, 2, 3 or 4;
X”'为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-或-NCH 3C(O)-。 X"' is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C (O) NCH3- , -NHC(O)- or -NCH3C (O)-.
本发明某些实施方式中，所述LA中，L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被选自-O-、-NH-、-C≡C-、-N(C 1-C 6烷基)-、-N(C 1-C 6卤代烷基)-、-N(C 1-C 6羟基烷基)-或-N(C 3-C 8环烷基)-替代，k为0、1、2、3、4、5、6或7。 In some embodiments of the present invention, in the LA, L 3 is -(CH 2 ) k , and one or two methylene groups in the L 3 are optionally selected from -O-, -NH-, -C≡C-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 - C8cycloalkyl )-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7.
优选的，本发明某些实施方式中，所述LA中，环A为键。Preferably, in some embodiments of the present invention, in the LA, ring A is a bond.
优选的，本发明某些实施方式中，所述LA中，环A为3-7元饱和或部分不饱和的亚环烷基、4-11元的饱和或部分不饱和的亚螺环烷基、4-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮、氧或硫杂原子的4-7元饱和或部分不饱和的亚杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮、氧或硫杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring A is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms.
优选的，本发明某些实施方式中，所述LA中，环A为3-6元饱和的亚环烷基或具有1个或2个独立地选自氮杂原子的4-7元饱和的单环亚杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring A is a 3-6 membered saturated cycloalkylene group or a 4-7 membered saturated cycloalkylene group with one or two nitrogen heteroatoms independently selected from nitrogen heteroatoms. Monocyclic heterocycloalkylene.
优选的，本发明某些实施方式中，所述LA中，环A为亚环己基(例如环己-1,4-二基，例如反式的环己-1,4-二基)、亚哌啶基(例如哌啶-1,4-二基)或亚哌嗪基(例如哌嗪-1,4-二基)。Preferably, in some embodiments of the present invention, in the LA, ring A is a cyclohexylene group (such as cyclohexylene-1,4-diyl, such as trans-cyclohexylene-1,4-diyl), a piperidinyl (eg piperidine-1,4-diyl) or piperazinylene (eg piperazine-1,4-diyl).
本发明某些实施方式中，所述LA中，环A为
Figure PCTCN2022088560-appb-000224
Figure PCTCN2022088560-appb-000225
其中a端与S连接，b端与X”'连接。 In some embodiments of the present invention, in the LA, ring A is
Figure PCTCN2022088560-appb-000224
Figure PCTCN2022088560-appb-000225
The a-end is connected to S, and the b-end is connected to X"'.
本发明某些实施方式中，所述LA中，环A为
Figure PCTCN2022088560-appb-000226
其中a端与S连接，b端与X”'连接。 In some embodiments of the present invention, in the LA, ring A is
Figure PCTCN2022088560-appb-000226
The a-end is connected to S, and the b-end is connected to X"'.
本发明某些实施方式中，所述LA中，环A为
Figure PCTCN2022088560-appb-000227
其中a端与S连接，b端与X”'连接。 In some embodiments of the present invention, in the LA, ring A is
Figure PCTCN2022088560-appb-000227
The a-end is connected to S, and the b-end is connected to X"'.
优选的，本发明某些实施方式中，所述LA中，环B为键。Preferably, in some embodiments of the present invention, in the LA, ring B is a bond.
优选的，本发明某些实施方式中，所述LA中，环B为3-7元饱和或部分不饱和的亚环烷基、4-11元的饱和或部分不饱和的亚螺环烷基、4-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮、氧或硫杂原子的4-7元饱和或部分不饱和的亚杂环烷基、具 有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮、氧或硫杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring B is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms.
优选的，本发明某些实施方式中，所述LA中，环B为含有1个或者2个氮杂原子的4－7元饱和的单环亚杂环烷基、含有1个或者2个氮杂原子的7-11元的亚螺杂环烷基或者亚稠杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring B is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, containing 1 or 2 nitrogens 7- to 11-membered spiroheterocycloalkylene or fused heterocycloalkylene of heteroatoms.
优选的，本发明某些实施方式中，所述LA中，环B为亚哌啶基(例如哌啶-1,4-二基)或亚哌嗪基(例如哌嗪-1,4-二基)。Preferably, in some embodiments of the present invention, in the LA, ring B is a piperidinide group (such as piperidine-1,4-diyl) or a piperazinide group (such as piperazine-1,4-diyl) base).
本发明某些实施方式中，所述LA中，环B为
Figure PCTCN2022088560-appb-000228
Figure PCTCN2022088560-appb-000229
其中c端与X”'连接，d端与L 3连接。 In some embodiments of the present invention, in the LA, ring B is
Figure PCTCN2022088560-appb-000228
Figure PCTCN2022088560-appb-000229
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
优选的，本发明某些实施方式中，环B为
Figure PCTCN2022088560-appb-000230
其中c端与X”'连接，d端与L 3连接。 Preferably, in some embodiments of the present invention, ring B is
Figure PCTCN2022088560-appb-000230
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
优选的，本发明某些实施方式中，所述LA中，环C为3-7元饱和或部分不饱和的亚环烷基、4-11元的饱和或部分不饱和的亚螺环烷基、4-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮、氧或硫杂原子的4-7元饱和或部分不饱和的亚杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的4-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮、氧或硫杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring C is a 3-7 membered saturated or partially unsaturated cycloalkylene, a 4-11 membered saturated or partially unsaturated spirocycloalkylene , 4-11-membered saturated or partially unsaturated fused cycloalkylene, 8-10-membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 4-7 membered saturated or partially unsaturated heterocycloalkylene, 4-11 membered saturated or partially unsaturated spiroheterocycloalkylene with 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur , 4-11-membered saturated or partially unsaturated fused heterocycloalkylene groups with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur 8- to 10-membered bicyclic saturated or partially unsaturated heterocycloalkylene of atoms.
优选的，本发明某些实施方式中，所述LA中，环C为含有1个或者2个氮杂原子的4－7元饱和的单环亚杂环烷基、含有1个或者2个氮杂原子的7-11元的亚螺杂环烷基或者亚稠杂环烷基。Preferably, in some embodiments of the present invention, in the LA, ring C is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, containing 1 or 2 nitrogens 7- to 11-membered spiroheterocycloalkylene or fused heterocycloalkylene of heteroatoms.
优选的，本发明某些实施方式中，所述LA中，环C为亚哌啶基(例如哌啶-1,4-二基)、亚哌嗪基(例如哌嗪-1,4-二基)、
Figure PCTCN2022088560-appb-000231
(例如
Figure PCTCN2022088560-appb-000232
)、
Figure PCTCN2022088560-appb-000233
(例如
Figure PCTCN2022088560-appb-000234
)、
Figure PCTCN2022088560-appb-000235
(例如
Figure PCTCN2022088560-appb-000236
)、
Figure PCTCN2022088560-appb-000237
(例如
Figure PCTCN2022088560-appb-000238
)、
Figure PCTCN2022088560-appb-000239
(例如
Figure PCTCN2022088560-appb-000240
)、
Figure PCTCN2022088560-appb-000241
(例如
Figure PCTCN2022088560-appb-000242
)、
Figure PCTCN2022088560-appb-000243
(例如
Figure PCTCN2022088560-appb-000244
)或
Figure PCTCN2022088560-appb-000245
(例如
Figure PCTCN2022088560-appb-000246
)。 Preferably, in some embodiments of the present invention, in the LA, ring C is a piperidinide group (such as piperidine-1,4-diyl), a piperazinide group (such as piperazine-1,4-diyl) base),
Figure PCTCN2022088560-appb-000231
(E.g
Figure PCTCN2022088560-appb-000232
),
Figure PCTCN2022088560-appb-000233
(E.g
Figure PCTCN2022088560-appb-000234
),
Figure PCTCN2022088560-appb-000235
(E.g
Figure PCTCN2022088560-appb-000236
),
Figure PCTCN2022088560-appb-000237
(E.g
Figure PCTCN2022088560-appb-000238
),
Figure PCTCN2022088560-appb-000239
(E.g
Figure PCTCN2022088560-appb-000240
),
Figure PCTCN2022088560-appb-000241
(E.g
Figure PCTCN2022088560-appb-000242
),
Figure PCTCN2022088560-appb-000243
(E.g
Figure PCTCN2022088560-appb-000244
)or
Figure PCTCN2022088560-appb-000245
(E.g
Figure PCTCN2022088560-appb-000246
).
本发明某些实施方式中，所述LA中，环C为
Figure PCTCN2022088560-appb-000247
Figure PCTCN2022088560-appb-000248
Figure PCTCN2022088560-appb-000249
其中e端与L 3连接，f端与X”连接。 In some embodiments of the present invention, in the LA, ring C is
Figure PCTCN2022088560-appb-000247
Figure PCTCN2022088560-appb-000248
Figure PCTCN2022088560-appb-000249
The e end is connected to L 3 and the f end is connected to X".
本发明某些实施方式中，所述LA中，环C为
Figure PCTCN2022088560-appb-000250
Figure PCTCN2022088560-appb-000251
其中e端与L 3连接，f端与X”连接。 In some embodiments of the present invention, in the LA, ring C is
Figure PCTCN2022088560-appb-000250
Figure PCTCN2022088560-appb-000251
The e end is connected to L 3 and the f end is connected to X".
优选的，本发明某些实施方式中，所述LA中环A为3-6元饱和的亚环烷基；环B含有1个或者2个氮杂原子的4-7元饱和的单环亚杂环烷基；环C为含有1个或者2个氮杂原子的4-7元饱和的单环亚杂环烷基、含有1个或者2个氮杂原子的7-11元的亚螺杂环烷基或者亚稠杂环烷基；X”为键或-C(O)-；L 3为-(CH 2) k，k为1、2、3、4或5(例如，k为1、2、3或4)。 Preferably, in some embodiments of the present invention, ring A in the LA is a 3-6 membered saturated cycloalkylene; ring B contains a 4-7 membered saturated monocyclic heteroatom with 1 or 2 nitrogen heteroatoms Cycloalkyl; Ring C is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, a 7-11 membered spiroheterocycle containing 1 or 2 nitrogen heteroatoms Alkyl or fused heterocycloalkylene; X" is a bond or -C(O)-; L 3 is -(CH 2 ) k , k is 1, 2, 3, 4 or 5 (for example, k is 1, 2, 3 or 4).
优选的，本发明某些实施方式中，所述LA中，X”为键或-C(O)-。Preferably, in some embodiments of the present invention, in the LA, X" is a bond or -C(O)-.
优选的，本发明某些实施方式中，所述LA中，X”为键。Preferably, in some embodiments of the present invention, in the LA, X" is a bond.
优选的，本发明某些实施方式中，所述LA中，X”为-C(O)-。Preferably, in some embodiments of the present invention, in the LA, X" is -C(O)-.
优选的，本发明某些实施方式中，所述LA中，X”为-C(O)CH 2O-。 Preferably, in some embodiments of the present invention, in the LA, X" is -C(O)CH 2 O-.
优选的，本发明某些实施方式中，所述LA中，X”'为键或-C(O)-。Preferably, in some embodiments of the present invention, in the LA, X"' is a bond or -C(O)-.
优选的，本发明某些实施方式中，所述LA中，X”'为键。Preferably, in some embodiments of the present invention, in the LA, X"' is a bond.
优选的，本发明某些实施方式中，所述LA中，X”'为-C(O)-。Preferably, in some embodiments of the present invention, in the LA, X"' is -C(O)-.
优选的，本发明某些实施方式中，所述LA中，k为1、2、3、4或5。Preferably, in some embodiments of the present invention, in the LA, k is 1, 2, 3, 4 or 5.
优选的，本发明某些实施方式中，所述LA中，L 3为-(CH 2) k，k为1、2、3、4或5。 Preferably, in some embodiments of the present invention, in the LA, L 3 is -(CH 2 ) k , and k is 1, 2, 3, 4 or 5.
优选的，本发明某些实施方式中，所述LA中，L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被-O-、-NH-、-C≡C-或-N(C 1-C 6烷基)-(例如-N(CH 3)-)替代，k为1、2、3、4或5。 Preferably, in some embodiments of the present invention, in the LA, L 3 is -(CH 2 ) k , and one or two methylene groups in the L 3 are optionally -O-, -NH- , -C≡C- or -N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-) substitution, and k is 1, 2, 3, 4 or 5.
优选的，本发明某些实施方式中，所述LA中，k为1、2、3或4。优选的，本发明某些实施方式中，所述LA中，L 3为-(CH 2) k-，其中所述L 3中包含的一个或两个CH 2各自独立地任选的被-O-、-NH-或-N(C 1-C 6烷基)-(例如-N(CH 3)-)替代，或者所述L 3中包含的一个-CH 2CH 2-任选的被-C≡C-替代；k为1、2、3或4。 Preferably, in some embodiments of the present invention, in the LA, k is 1, 2, 3 or 4. Preferably, in some embodiments of the present invention, in the LA, L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently optionally -O -, -NH- or -N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-) is replaced, or one -CH 2 CH 2 - contained in said L 3 is optionally - C≡C-substitution; k is 1, 2, 3, or 4.
优选的，本发明某些实施方式中，所述LA中，L 3为-(CH 2) k-，所述L 3中的一个亚甲基任选的被-O-、-NH-或-N(C 1-C 6烷基)-(例如-N(CH 3)-)的基团替代；k为1、2、3或4。 Preferably, in some embodiments of the present invention, in the LA, L 3 is -(CH 2 ) k -, and a methylene group in the L 3 is optionally -O-, -NH- or - Group substitution of N(C 1 -C 6 alkyl)- (eg -N(CH 3 )-); k is 1, 2, 3 or 4.
优选的，本发明某些实施方式中，所述LA为LA-1：Preferably, in some embodiments of the present invention, the LA is LA-1:
Figure PCTCN2022088560-appb-000252
Figure PCTCN2022088560-appb-000252
其中所述环A、环B、环C、L 3、X”如LA中所定义和描述。 wherein said Ring A , Ring B, Ring C, L3, X" are as defined and described in LA.
本发明某些实施方式中，所述LA为LA-2：In certain embodiments of the present invention, the LA is LA-2:
Figure PCTCN2022088560-appb-000253
Figure PCTCN2022088560-appb-000253
Figure PCTCN2022088560-appb-000254
Figure PCTCN2022088560-appb-000254
其中，环A为
Figure PCTCN2022088560-appb-000255
Figure PCTCN2022088560-appb-000256
其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代； where ring A is
Figure PCTCN2022088560-appb-000255
Figure PCTCN2022088560-appb-000256
wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
X”'为-C(O)-；X"' is -C(O)-;
环B为
Figure PCTCN2022088560-appb-000257
其中c端与X”'连接，d端与L 3连接；所述环B中的1、2、3或4个氢原子任选被F取代； Ring B is
Figure PCTCN2022088560-appb-000257
wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
L 3为-(CH 2) k-，其中所述L 3中包含的一个或两个CH 2各自独立地任选的被-O-、-NH-或-N(C 1-C 6烷基)-(例如-N(CH 3)-)替代，或者所述L 3中包含的一个-CH 2CH 2-任选的被-C≡C-替代；k为1、2、3或4； L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in said L 3 are each independently optionally -O-, -NH- or -N(C 1 -C 6 alkyl )- (eg -N(CH 3 )-) is replaced, or one -CH 2 CH 2 - contained in the L 3 is optionally replaced by -C≡C-; k is 1, 2, 3 or 4;
环C为
Figure PCTCN2022088560-appb-000258
其中e端与L 3连接，f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代； Ring C is
Figure PCTCN2022088560-appb-000258
Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
X”为-C(O)-。X" is -C(O)-.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-2中，环A为
Figure PCTCN2022088560-appb-000259
Figure PCTCN2022088560-appb-000260
其中a端与S连接，b端与X”'连接。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-2, ring A is
Figure PCTCN2022088560-appb-000259
Figure PCTCN2022088560-appb-000260
The a-end is connected to S, and the b-end is connected to X"'.
优选的，本发明某些实施方式中，环B为
Figure PCTCN2022088560-appb-000261
其中c端与X”'连接，d端与L 3连接。 Preferably, in some embodiments of the present invention, ring B is
Figure PCTCN2022088560-appb-000261
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
本发明某些实施方式中，所述LA、LA-1和LA-2中，L 3为-(CH 2) k-，其中所述L 3中包含的一个或两个CH 2各自独立地任选的被-O-、-NH-或-N(CH 3)-替代；k为1、2、3或4。 In some embodiments of the present invention, in the LA, LA-1 and LA-2, L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently any Optionally replaced by -O-, -NH- or -N( CH3 )-; k is 1, 2, 3 or 4.
本发明某些实施方式中，所述LA、LA-1和LA-2中，L 3为-(CH 2) k-，其中所述L 3中包含的一个或两个CH 2各自独立地任选的被-O-替代；k为1、2、3或4。 In some embodiments of the present invention, in the LA, LA-1 and LA-2, L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in the L 3 are each independently any Selected is replaced by -O-; k is 1, 2, 3 or 4.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-2中，k为3或4，优选为4。Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-2, k is 3 or 4, preferably 4.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-2中，L 3为-(CH 2) k-，其中所述L 3中包含的一个CH 2任选的被-O-替代；k为4。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-2, L 3 is -(CH 2 ) k -, wherein one CH 2 contained in the L 3 is optionally -O- substitution; k is 4.
本发明某些实施方式中，所述LA、LA-1和LA-2中，L 3可为-CH 2-、-(CH 2) 2-、-(CH 2) 3-、-(CH 2) 4-、
Figure PCTCN2022088560-appb-000262
Figure PCTCN2022088560-appb-000263
其中k”端与环B连接，k'端与环C连接。 In some embodiments of the present invention, in the LA, LA-1 and LA-2, L 3 can be -CH 2 -, -(CH 2 ) 2 -, -(CH 2 ) 3 -, -(CH 2 ) 4- ,
Figure PCTCN2022088560-appb-000262
Figure PCTCN2022088560-appb-000263
The k" end is connected to ring B, and the k' end is connected to ring C.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-2中，L 3可为-(CH 2) 4-、
Figure PCTCN2022088560-appb-000264
Figure PCTCN2022088560-appb-000265
Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-2, L 3 can be -(CH 2 ) 4 -,
Figure PCTCN2022088560-appb-000264
Figure PCTCN2022088560-appb-000265
优选的，本发明某些实施方式中，所述LA、LA-1和LA-2中，环C为
Figure PCTCN2022088560-appb-000266
Figure PCTCN2022088560-appb-000267
其中e端与L 3连接，f端与X”连接。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-2, ring C is
Figure PCTCN2022088560-appb-000266
Figure PCTCN2022088560-appb-000267
The e end is connected to L 3 and the f end is connected to X".
本发明某些实施方式中，所述LA-2为如下任一结构：In certain embodiments of the present invention, the LA-2 is any of the following structures:
Figure PCTCN2022088560-appb-000268
Figure PCTCN2022088560-appb-000268
Figure PCTCN2022088560-appb-000269
Figure PCTCN2022088560-appb-000269
优选的，本发明某些实施方式中，所述LA-2为如下任一结构：Preferably, in some embodiments of the present invention, the LA-2 is any of the following structures:
Figure PCTCN2022088560-appb-000270
Figure PCTCN2022088560-appb-000271
Figure PCTCN2022088560-appb-000270
Figure PCTCN2022088560-appb-000271
本发明某些实施方式中，所述LA为LA-3：In certain embodiments of the present invention, the LA is LA-3:
Figure PCTCN2022088560-appb-000272
Figure PCTCN2022088560-appb-000272
其中，环A为
Figure PCTCN2022088560-appb-000273
Figure PCTCN2022088560-appb-000274
其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代； where ring A is
Figure PCTCN2022088560-appb-000273
Figure PCTCN2022088560-appb-000274
wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
X”'为-C(O)-；X"' is -C(O)-;
环B为
Figure PCTCN2022088560-appb-000275
其中c端与X”'连接，d端与L 3连接；所述环B中的1、2、3或4个氢原子任选被F取代； Ring B is
Figure PCTCN2022088560-appb-000275
wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
L 3为-(CH 2) k-，其中所述L 3中包含的一个CH 2任选的被-O-、-NH-或-N(C 1-C 6烷基)-(例如-N(CH 3)-)替代；k为1或2； L 3 is -(CH 2 ) k -, wherein one CH 2 contained in said L 3 is optionally -O-, -NH- or -N(C 1 -C 6 alkyl)- (eg -N (CH 3 )-) substitution; k is 1 or 2;
环C为
Figure PCTCN2022088560-appb-000276
其中e端与L 3连接，f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代； Ring C is
Figure PCTCN2022088560-appb-000276
Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
X”为-C(O)-。X" is -C(O)-.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-3中，环A为
Figure PCTCN2022088560-appb-000277
Figure PCTCN2022088560-appb-000278
优选为
Figure PCTCN2022088560-appb-000279
其中a端与S连接，b端与X”'连接。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-3, ring A is
Figure PCTCN2022088560-appb-000277
Figure PCTCN2022088560-appb-000278
preferably
Figure PCTCN2022088560-appb-000279
The a-end is connected to S, and the b-end is connected to X"'.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-3中，环B为
Figure PCTCN2022088560-appb-000280
Figure PCTCN2022088560-appb-000281
其中c端与X”'连接，d端与L 3连接。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-3, ring B is
Figure PCTCN2022088560-appb-000280
Figure PCTCN2022088560-appb-000281
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-3中，L 3为-(CH 2) k-，k为1或2。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-3, L 3 is -(CH 2 ) k -, and k is 1 or 2.
优选的，本发明某些实施方式中，所述LA、LA-1和LA-3中，环C为
Figure PCTCN2022088560-appb-000282
Figure PCTCN2022088560-appb-000283
其中c端与X”'连接，d端与L 3连接。 Preferably, in some embodiments of the present invention, in the LA, LA-1 and LA-3, ring C is
Figure PCTCN2022088560-appb-000282
Figure PCTCN2022088560-appb-000283
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
本发明某些实施方式中，所述LA-3为如下任一结构：In certain embodiments of the present invention, the LA-3 is any of the following structures:
Figure PCTCN2022088560-appb-000284
Figure PCTCN2022088560-appb-000284
优选的，本发明某些实施方式中，所述LA-3为如下任一结构：Preferably, in some embodiments of the present invention, the LA-3 is any of the following structures:
Figure PCTCN2022088560-appb-000285
Figure PCTCN2022088560-appb-000285
本发明某些实施方式中，所述LA为LA-4：In certain embodiments of the present invention, the LA is LA-4:
Figure PCTCN2022088560-appb-000286
Figure PCTCN2022088560-appb-000286
其中，环A为
Figure PCTCN2022088560-appb-000287
Figure PCTCN2022088560-appb-000288
其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代； where ring A is
Figure PCTCN2022088560-appb-000287
Figure PCTCN2022088560-appb-000288
wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
X”'为键、-C(O)NH-或-C(O)NCH 3-； X"' is a bond, -C(O)NH- or -C(O)NCH 3 -;
环B为键；Ring B is a bond;
L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被-O-、-NH-、-C(O)-、-C≡C-或-N(C 1-C 6烷基)-替代，k为0、1、2、3、4、5、6或7； L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally -O-, -NH-, -C(O)-, -C≡C- or -N (C 1 -C 6 alkyl)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
环C为
Figure PCTCN2022088560-appb-000289
Figure PCTCN2022088560-appb-000290
其中e端与L 3连接， f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代； Ring C is
Figure PCTCN2022088560-appb-000289
Figure PCTCN2022088560-appb-000290
Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
X”为-C(O)-。X" is -C(O)-.
本发明某些实施方式中，所述LA-4中，环A为
Figure PCTCN2022088560-appb-000291
其中a端与S连接，b端与X”'连接。 In some embodiments of the present invention, in the LA-4, ring A is
Figure PCTCN2022088560-appb-000291
The a-end is connected to S, and the b-end is connected to X"'.
本发明某些实施方式中，所述LA-4中，L 3为-CH 2-、
Figure PCTCN2022088560-appb-000292
Figure PCTCN2022088560-appb-000293
其中k”端与环B连接，k'端与环C连接。 In some embodiments of the present invention, in the LA-4, L 3 is -CH 2 -,
Figure PCTCN2022088560-appb-000292
Figure PCTCN2022088560-appb-000293
The k" end is connected to ring B, and the k' end is connected to ring C.
本发明某些实施方式中，所述LA-4中，环C为
Figure PCTCN2022088560-appb-000294
其中e端与L 3连接，f端与X”连接。 In some embodiments of the present invention, in the LA-4, ring C is
Figure PCTCN2022088560-appb-000294
The e end is connected to L 3 and the f end is connected to X".
本发明某些实施方式中，所述LA-4为如下任一结构：In certain embodiments of the present invention, the LA-4 is any of the following structures:
Figure PCTCN2022088560-appb-000295
Figure PCTCN2022088560-appb-000295
优选的，本发明某些实施方式中，所述LA-4为如下任一结构：Preferably, in some embodiments of the present invention, the LA-4 is any of the following structures:
Figure PCTCN2022088560-appb-000296
Figure PCTCN2022088560-appb-000296
本发明某些实施方式中，所述LA为LA-5：In certain embodiments of the present invention, the LA is LA-5:
Figure PCTCN2022088560-appb-000297
Figure PCTCN2022088560-appb-000297
其中，环A、X”'、环B、L 3和环C如LA-2或LA-3所定义； wherein Ring A, X''', Ring B, L 3 and Ring C are as defined in LA-2 or LA-3;
X”为-C(O)CH 2O-，X”中的-C(O)-与环C连接。 X" is -C(O)CH 2 O-, and -C(O)- in X" is connected to ring C.
本发明某些实施方式中，所述LA-5中，环A为
Figure PCTCN2022088560-appb-000298
其中a端与S连接，b端与X”'连接。 In some embodiments of the present invention, in the LA-5, ring A is
Figure PCTCN2022088560-appb-000298
The a-end is connected to S, and the b-end is connected to X"'.
本发明某些实施方式中，所述LA-5中，环B为
Figure PCTCN2022088560-appb-000299
其中c端与X”'连接，d端与L 3连接。 In some embodiments of the present invention, in the LA-5, ring B is
Figure PCTCN2022088560-appb-000299
Wherein the c-terminal is connected with X''', and the d - terminal is connected with L3.
本发明某些实施方式中，所述LA-5中，L 3为-(CH 2) k，k为1或2，优选为1。 In some embodiments of the present invention, in the LA-5, L 3 is -(CH 2 ) k , and k is 1 or 2, preferably 1.
本发明某些实施方式中，所述LA-5中，环C为
Figure PCTCN2022088560-appb-000300
其中e端与L 3连接，f端与X”连接。 In some embodiments of the present invention, in the LA-5, ring C is
Figure PCTCN2022088560-appb-000300
The e end is connected to L 3 and the f end is connected to X".
优选的，本发明某些实施方式中，所述LA-5为Preferably, in some embodiments of the present invention, the LA-5 is
Figure PCTCN2022088560-appb-000301
Figure PCTCN2022088560-appb-000301
优选的，本发明某些实施方式中，所述LA为Preferably, in some embodiments of the present invention, the LA is
Figure PCTCN2022088560-appb-000302
Figure PCTCN2022088560-appb-000302
Figure PCTCN2022088560-appb-000303
Figure PCTCN2022088560-appb-000303
Figure PCTCN2022088560-appb-000304
Figure PCTCN2022088560-appb-000304
优选的，本发明某些实施方式中，所述E为CRBN、VHL、XAIP或者MDM2E3泛素连接酶小分子配体。Preferably, in some embodiments of the present invention, the E is a small molecule ligand of CRBN, VHL, XAIP or MDM2E3 ubiquitin ligase.
优选的，本发明某些实施方式中，所述E为E1、E1a、E1b或者E1cPreferably, in some embodiments of the present invention, the E is E1, E1a, E1b or E1c
Figure PCTCN2022088560-appb-000305
Figure PCTCN2022088560-appb-000305
Figure PCTCN2022088560-appb-000306
Figure PCTCN2022088560-appb-000306
其中所述E1、E1a、E1b或E1c、：wherein said E1, E1a, E1b or E1c,:
每个R 1各自独立的为卤素、任选取代的酰基、任选取代的烷基、任选取代的烯基、任选取代的炔基、任选取代的碳环、任选取代的杂环、任选取代的芳基、任选取代杂芳基、-CN或者-O(CH 2) XR 1A； Each R is independently halogen , optionally substituted acyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocycle, optionally substituted heterocycle , optionally substituted aryl, optionally substituted heteroaryl, -CN or -O(CH 2 ) X R 1A ;
且至少有一个R 1为-O(CH 2) xR 1A； and at least one R 1 is -O(CH 2 ) x R 1A ;
R 6是未取代异丙基、-(CH 2)C(O)OMe，或者-(CH 2) 2OH； R 6 is unsubstituted isopropyl, -(CH 2 )C(O)OMe, or -(CH 2 ) 2 OH;
R 6A是取代的烷基； R 6A is substituted alkyl;
R 7是氢、任选取代的酰基、任选取代的烷基或者氮保护基； R 7 is hydrogen, optionally substituted acyl, optionally substituted alkyl, or nitrogen protecting group;
R 1A为氢、任选取代的烷基、任选取代的烯基、任选取代的炔基、任选取代的碳环、任选取代的杂环、任选取代的芳基、任选取代的杂芳基、-OR A、-N(R B) 2、或者-SR A； R 1A is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocycle, optionally substituted heterocycle, optionally substituted aryl, optionally substituted of heteroaryl, -OR A , -N(R B ) 2 , or -SR A ;
每个R A各自独立的为氢、任选取代的酰基、任选取代的烷基、且当连接至O是为氧保护基、当连接至S时为硫保护基； Each R A is independently hydrogen, optionally substituted acyl, optionally substituted alkyl, and when attached to O is an oxygen protecting group and when attached to S is a sulfur protecting group;
每个R B各自独立的为氢、任选取代的酰基、任选取代的烷基、氮保护基； each R is independently hydrogen, optionally substituted acyl, optionally substituted alkyl, nitrogen protecting group;
n为1、2、3或4；且n is 1, 2, 3, or 4; and
x为0、1、2、3、4、5或者6，且当R 6是异丙基，R 6A是甲基，R 7是氢，n为1时，R 1不是甲基或者羟基甲基。 x is 0, 1, 2, 3, 4, 5, or 6 , and when R6 is isopropyl, R6A is methyl, R7 is hydrogen, and n is 1 , R1 is not methyl or hydroxymethyl .
优选的，本发明某些实施方式中，所述E为E2Preferably, in some embodiments of the present invention, the E is E2
Figure PCTCN2022088560-appb-000307
Figure PCTCN2022088560-appb-000307
其中所述E2中：where the E2:
X 101为键、-CH 2-、-CHCF 3-、-S(O) 2-、-S(O)-、-P(O)R 100-、-P(O)OR 100-、-P(O)N(R 100) 2、-C(O)-、-C(S)-、或者
Figure PCTCN2022088560-appb-000308
X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
Figure PCTCN2022088560-appb-000308
X 201为C或者Si； X 201 is C or Si;
X 301为-CH 2-、-O-、-S-、-C(R 100) 2-或-Si(R 100) 2-； X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
R 101选自氢、氘、卤素、-CN、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-P(O)(OR 100) 2、-P(O)[N(R 100) 2](OR 100)、-P(O)[N(R 100) 2] 2、-Si(OH) 2(R 100)-、-Si(OH)(R 100) 2-、-Si(R 100) 3-、或者任选被取代的C 1- C 4烷基； R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
R 201选自氢、-R 601、卤素、-CN、-NO 2、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-S(O) 2N(R 100) 2、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100)2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2、-OP(O)(R 100) 2、-OP(O)(OR 100) 2、-OP(O)(OR 100)[N(R 100) 2]、-OP(O)[N(R 100) 2]、-NP(O)(R 100) 2、-NR 100P(O)(OR 100) 2、-N(R 100)P(O)(OR 100)[N(R 100) 2]、-N(R 100)P(O)[N(R 100) 2] 2、或-NR 100S(O) 2R 100； R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP( O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N(R 100 ) 2 ], -OP(O)[N(R 100 ) 2 ] , -NP(O)(R 100 ) 2 , -NR 100 P(O)(OR 100 ) 2 , -N(R 100 )P(O)(OR 100 )[N(R 100 ) 2 ], -N (R 100 )P(O)[N(R 100 ) 2 ] 2 , or -NR 100 S(O) 2 R 100 ;
L 101为键或C 1-C 4亚烷基，所述C 1-C 4亚烷基中1个或2亚甲基任选被选去-O-、-C(O)-、-C(S)-、-C(R 100) 2-、-CH(R 100)-、-C(F) 2-、-N(R 100)-、-S-、-S(O) 2-或者-CH＝CH替代； L 101 is a bond or a C 1 -C 4 alkylene group, and 1 or 2 methylene groups in the C 1 -C 4 alkylene group are optionally selected to remove -O-, -C(O)-, -C (S)-, -C(R 100 ) 2 -, -CH(R 100 )-, -C(F) 2 -, -N(R 100 )-, -S-, -S(O) 2 - or -CH=CH substitution;
环A为双环或三环，选自Ring A is bicyclic or tricyclic, selected from
Figure PCTCN2022088560-appb-000309
Figure PCTCN2022088560-appb-000309
Figure PCTCN2022088560-appb-000310
Figure PCTCN2022088560-appb-000310
Figure PCTCN2022088560-appb-000311
Figure PCTCN2022088560-appb-000311
Figure PCTCN2022088560-appb-000312
Figure PCTCN2022088560-appb-000312
Figure PCTCN2022088560-appb-000313
Figure PCTCN2022088560-appb-000313
其中：in:
环B为含有1-2个N原子的6-元杂芳基、苯基、5-7元饱和或部分不饱和的环烷基、含有1-2个选自N、O、S杂原子的5-7元饱和或部分不饱和的杂环烷基、或者含有1-3个选自N、O、S杂原子的5元杂芳基；Ring B is a 6-membered heteroaryl group containing 1-2 N atoms, a phenyl group, a 5-7 membered saturated or partially unsaturated cycloalkyl group, a group containing 1-2 heteroatoms selected from N, O, and S. 5-7-membered saturated or partially unsaturated heterocycloalkyl, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, and S;
R 301选自氢、卤素、-OR 100、-SR 100或-N(R 100) 2； R 301 is selected from hydrogen, halogen, -OR 100 , -SR 100 or -N(R 100 ) 2 ;
R 401为氢、-R 601、-卤素、-CN、硝基、-OR 100、-SR 100、-N(R 100) 2、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-S(O) 2N(R 100) 2、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100)2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2或-NR 100S(O) 2R 100； R 401 is hydrogen, -R 601 , -halogen, -CN, nitro, -OR 100 , -SR 100 , -N(R 100 ) 2 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 or -NR 100 S(O) 2 R 100 ;
R 501为氢、-CN或C 1-C 4烷基； R 501 is hydrogen, -CN or C 1 -C 4 alkyl;
R 601为任选取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或者部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基； R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
R 100选自氢、任选被取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基，或者的两个R 100与其相连接的N原子一起形成除了连接N原子之外还含有0-3个选自N、O或S杂原子的饱和的或部分不饱和的4-7元杂芳基； R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 saturated or partially unsaturated 4-7 membered heteroaryl groups selected from N, O or S heteroatoms;
m”为0、1、2、3或4。m" is 0, 1, 2, 3 or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E3：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E3:
Figure PCTCN2022088560-appb-000314
Figure PCTCN2022088560-appb-000314
其中所述：which states:
X 101为键、-CH 2-、-CHCF 3-、-S(O) 2-、-S(O)-、-P(O)R 100-、-P(O)OR 100-、-P(O)N(R 100) 2、-C(O)-、-C(S)-、或者
Figure PCTCN2022088560-appb-000315
X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
Figure PCTCN2022088560-appb-000315
X 201为C、N或者Si； X 201 is C, N or Si;
X 301为-CH 2-、-O-、-S-、-C(R 100) 2-或-Si(R 100) 2-； X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
R 101选自氢、氘、卤素、-CN、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-P(O)(OR 100) 2、- P(O)[N(R 100) 2](OR 100)、-P(O)[N(R 100) 2] 2、-Si(OH) 2(R 100)-、-Si(OH)(R 100) 2-、-Si(R 100) 3-、或者任选被取代的C 1-C 4烷基； R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
L 101为键或C 1-C 4亚烷基，所述C 1-C 4亚烷基中1个或2亚甲基任选被选去-O-、-C(O)-、-C(S)-、-C(R 100) 2-、-CH(R 100)-、-C(F) 2-、-N(R 100)-、-S-、-S(O) 2-或者-CH＝CH替代； L 101 is a bond or a C 1 -C 4 alkylene group, and 1 or 2 methylene groups in the C 1 -C 4 alkylene group are optionally selected to remove -O-, -C(O)-, -C (S)-, -C(R 100 ) 2 -, -CH(R 100 )-, -C(F) 2 -, -N(R 100 )-, -S-, -S(O) 2 - or -CH=CH substitution;
环A不存在或为单环或者双环，选自：Ring A is absent or monocyclic or bicyclic, selected from:
Figure PCTCN2022088560-appb-000316
Figure PCTCN2022088560-appb-000316
Figure PCTCN2022088560-appb-000317
Figure PCTCN2022088560-appb-000317
Figure PCTCN2022088560-appb-000318
Figure PCTCN2022088560-appb-000318
R 201选自氢、-R 601、卤素、-CN、-NO 2、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-S(O) 2NR 100、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100)2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2、-OP(O)(R 100) 2、-OP(O)(OR 100) 2、-OP(O)(OR 100)[N(R 100) 2]、-OP(O)[N(R 100) 2]、-NP(O)(R 100) 2、-NR 100P(O)(OR 100) 2、-N(R 100)P(O)(OR 100)[N(R 100) 2]、-N(R 100)P(O)[N(R 100) 2] 2、或-NR 100S(O) 2R 100； R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC( O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP(O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N(R 100 ) 2 ], -OP(O)[N(R 100 ) 2 ], -NP( O)(R 100 ) 2 , -NR 100 P(O)(OR 100 ) 2 , -N(R 100 )P(O)(OR 100 )[N(R 100 ) 2 ], -N(R 100 ) P(O)[N(R 100 ) 2 ] 2 , or -NR 100 S(O) 2 R 100 ;
环B为含有1-2个N原子的6-元杂芳基、苯基、5-7元饱和或部分不饱和的环烷基、含有1-2个选自N、O、S杂原子的5-7元饱和或部分不饱和的杂环烷基、或者含有1-3个选自N、O、S杂原子的5元杂芳基；Ring B is a 6-membered heteroaryl group containing 1-2 N atoms, a phenyl group, a 5-7 membered saturated or partially unsaturated cycloalkyl group, a group containing 1-2 heteroatoms selected from N, O, and S. 5-7-membered saturated or partially unsaturated heterocycloalkyl, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, and S;
R 301和R 401各自独立的为氢、-R 601、卤素、-CN、-NO 2、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-S(O) 2NR 100、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100)2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2或-NR 100S(O) 2R 100； R 301 and R 401 are each independently hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , - N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 or -NR 100 S(O) 2 R 100 ;
R 501为氢、-CN或C 1-C 4烷基； R 501 is hydrogen, -CN or C 1 -C 4 alkyl;
R 601为任选取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或者部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基； R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
R 100选自氢、任选被取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基，或者的两个R 100与其相连接的N原子一起形成除了连接N原子之外还含有0-3个选自N、O或S的杂原子； R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 heteroatoms selected from N, O or S;
P”为0或1；P" is 0 or 1;
m”为0、1或2；m" is 0, 1 or 2;
n”为0、1、2、3或4。n" is 0, 1, 2, 3 or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E4：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E4:
Figure PCTCN2022088560-appb-000319
Figure PCTCN2022088560-appb-000319
其中所述E4中：where the E4:
X 101为键、-CH 2-、-CHCF 3-、-S(O) 2-、-S(O)-、-P(O)R 100-、-P(O)OR 100-、-P(O)N(R 100) 2、-C(O)-、-C(S)-、或者
Figure PCTCN2022088560-appb-000320
X 101 is a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P (O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
Figure PCTCN2022088560-appb-000320
X 201为C、N或者Si； X 201 is C, N or Si;
X 301为-CH 2-、-O-、-S-、-C(R 100) 2-或-Si(R 100) 2-； X 301 is -CH 2 -, -O-, -S-, -C(R 100 ) 2 - or -Si(R 100 ) 2 -;
R 101选自氢、氘、卤素、-CN、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-P(O)(OR 100) 2、-P(O)[N(R 100) 2](OR 100)、-P(O)[N(R 100) 2] 2、-Si(OH) 2(R 100)-、-Si(OH)(R 100) 2-、-Si(R 100) 3-、或者任选被取代的C 1-C 4烷基； R 101 is selected from hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O )(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 ) -, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C 1 -C 4 alkyl;
L 101为键或C 1-C 4亚烷基，所述C 1-C 4亚烷基中1个或2亚甲基任选被选去-O-、-C(O)-、-C(S)-、-C(R 100) 2-、-CH(R 100)-、-C(F) 2-、-N(R 100)-、-S-、-S(O) 2-或者-CH＝CH替代； L 101 is a bond or a C 1 -C 4 alkylene group, and 1 or 2 methylene groups in the C 1 -C 4 alkylene group are optionally selected to remove -O-, -C(O)-, -C (S)-, -C(R 100 ) 2 -, -CH(R 100 )-, -C(F) 2 -, -N(R 100 )-, -S-, -S(O) 2 - or -CH=CH substitution;
R 201选自氢、-R 601、卤素、-CN、-NO 2、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-S(O) 2NR 100、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100)2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2、-OP(O)(R 100) 2、-OP(O)(OR 100) 2、-OP(O)(OR 100)[N(R 100) 2]、-OP(O)[N(R 100) 2]、-NP(O)(R 100) 2、-NR 100P(O)(OR 100) 2、-N(R 100)P(O)(OR 100)[N(R 100) 2]、-N(R 100)P(O)[N(R 100) 2] 2、或-NR 100S(O) 2R 100； R 201 is selected from hydrogen, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -S(O) 2 NR 100 , -C(O)R 100 , -C(O)OR 100 , -C(O)N(R 100)2 , -OC(O)R 100 , -OC( O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP(O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N(R 100 ) 2 ], -OP(O)[N(R 100 ) 2 ], -NP( O)(R 100 ) 2 , -NR 100 P(O)(OR 100 ) 2 , -N(R 100 )P(O)(OR 100 )[N(R 100 ) 2 ], -N(R 100 ) P(O)[N(R 100 ) 2 ] 2 , or -NR 100 S(O) 2 R 100 ;
R 601为任选取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或者部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基； R 601 is optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, containing 1-4 5-6 membered heteroaryl groups selected from N, O or S heteroatoms;
R 100选自氢、任选被取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基，或者的两个R 100与其相连接的N原子一起形成除了连接N原子之外还含有0-3个选自N、O或S杂原子的； R 100 is selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycle containing 1-2 heteroatoms selected from N, O or S Alkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S, or two R 100 together with the N atom to which it is attached to form a 0- 3 heteroatoms selected from N, O or S;
环E、环F和环G各自独立的为含有1-2个N原子的6-元杂芳基、苯基、5-7元饱和或部分不饱和的环烷基、含有1-2个选自N、O、S杂原子的5-7元饱和或部分不饱和的杂环烷基、或者含有1-3个选自N、O、S杂原子的5元杂芳基；Ring E, Ring F and Ring G are each independently a 6-membered heteroaryl containing 1-2 N atoms, a phenyl, a 5-7 membered saturated or partially unsaturated cycloalkyl, containing 1-2 optional 5-7-membered saturated or partially unsaturated heterocycloalkyl from N, O, S heteroatoms, or 5-membered heteroaryl containing 1-3 heteroatoms selected from N, O, S;
m”为0、1、2、3、4、5、6、7、8、9、10、11、12、13、14、15或16。m" is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or 16.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E5：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E5:
Figure PCTCN2022088560-appb-000321
Figure PCTCN2022088560-appb-000321
其中所述E5中：环M选自
Figure PCTCN2022088560-appb-000322
Figure PCTCN2022088560-appb-000323
或者
Figure PCTCN2022088560-appb-000324
In wherein said E5: ring M is selected from
Figure PCTCN2022088560-appb-000322
Figure PCTCN2022088560-appb-000323
or
Figure PCTCN2022088560-appb-000324
每个X 101、X 601和X 701各自独立的为键、-CH 2-、-CHCF 3-、-S(O) 2-、-S(O)-、-P(O)R 100-、-P(O)OR 100-、-P(O)N(R 100) 2、-C(O)-、-C(S)-、或者
Figure PCTCN2022088560-appb-000325
Each of X 101 , X 601 and X 701 is independently a bond, -CH 2 -, -CHCF 3 -, -S(O) 2 -, -S(O)-, -P(O)R 100 -, -P(O)OR 100 -, -P(O)N(R 100 ) 2 , -C(O)-, -C(S)-, or
Figure PCTCN2022088560-appb-000325
每个X 301和X 501各自独立的为键、-C(R 100) 2-、-NR 100-、-O-、-S-、或者-Si(R 100) 2-； Each X 301 and X 501 is independently a bond, -C(R 100 ) 2 -, -NR 100 -, -O-, -S-, or -Si(R 100 ) 2 -;
X 401选自
Figure PCTCN2022088560-appb-000326
X 401 from
Figure PCTCN2022088560-appb-000326
每个R 100各自独立的选自氢、任选被取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基，或者的两个R 100与其相连接的N原子一起形成除了连接N原子之外还含有0-3个选自N、O或S杂原子的； Each R 100 is independently selected from hydrogen, optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially containing 1-2 heteroatoms selected from N, O or S Unsaturated heterocycloalkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O, or S, or two R 100 together with the N atom to which it is attached form except the one to which the N atom is attached. Also contains 0-3 heteroatoms selected from N, O or S;
每个R 301a各自独立的为氢、氘、-R 601、卤素、-CN、-NO 2、-OR 100、-SR 100、-N(R 100) 2、-Si(R 100) 3、-S(O)R 100、-S(O) 2R 100、-S(O) 2N(R 100) 2、-C(O)R 100、-C(O)OR 100、-C(O)N(R 100) 2、-C(O)N(R 100)OR 100、-C(R 100) 2N(R 100)C(O)R 100、-C(R 100) 2N(R 100)C(O)N(R 100) 2、-OC(O)R 100、-OC(O)N(R 100) 2、-NR 100C(O)OR 100、-NR 100C(O)R 100、-NR 100C(O)N(R 100) 2、-OP(O)(R 100) 2、-OP(O)(OR 100) 2、-OP(O)(OR 100)[N(R 100) 2]、-OP(O)[N(R 100) 2]、-NP(O)(R 100) 2、-NR 100P(O)(OR 100) 2、-N(R 100)P(O)(OR 100)[N(R 100) 2]、-N(R 100)P(O)[N(R 100) 2] 2、或-NR 100S(O) 2R 100； Each R 301a is independently hydrogen, deuterium, -R 601 , halogen, -CN, -NO 2 , -OR 100 , -SR 100 , -N(R 100 ) 2 , -Si(R 100 ) 3 , - S(O)R 100 , -S(O) 2 R 100 , -S(O) 2 N(R 100 ) 2 , -C(O)R 100 , -C(O)OR 100 , -C(O) N(R 100 ) 2 , -C(O)N(R 100 )OR 100 , -C(R 100 ) 2 N(R 100 )C(O)R 100 , -C(R 100 ) 2 N(R 100 )C(O)N(R 100 ) 2 , -OC(O)R 100 , -OC(O)N(R 100 ) 2 , -NR 100 C(O)OR 100 , -NR 100 C(O)R 100 , -NR 100 C(O)N(R 100 ) 2 , -OP(O)(R 100 ) 2 , -OP(O)(OR 100 ) 2 , -OP(O)(OR 100 )[N( R 100 ) 2 ], -OP(O)[N(R 100 ) 2 ], -NP(O)(R 100 ) 2 , -NR 100 P(O)(OR 100 ) 2 , -N(R 100 ) P(O)(OR 100 )[N(R 100 ) 2 ], -N(R 100 )P(O)[N(R 100 ) 2 ] 2 , or -NR 100 S(O) 2 R 100 ;
每个R 601各自独立的为任选取代的C 1-C 6烷基、苯基、含有1-2个选自N、O或S杂原子的4-7元饱和的或者部分不饱和的杂环烷基、含有1-4个选自N、O或S杂原子的5-6元杂芳基； Each R 601 is independently optionally substituted C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heteroatoms containing 1-2 heteroatoms selected from N, O or S. Cycloalkyl, 5-6 membered heteroaryl containing 1-4 heteroatoms selected from N, O or S;
每个R 701各自独立的为氢、氘、卤素、-CN、-OR 100、-SR 100、-S(O)R 100、-S(O) 2R 100、-N(R 100) 2、-P(O)(OR 100) 2、-P(O)[N(R 100) 2](OR 100)、-P(O)[N(R 100) 2] 2、-Si(OH) 2(R 100)-、-Si(OH)(R 100) 2-、-Si(R 100) 3-、或者任选被取代的 C1-C4烷基；或者 Each R 701 is independently hydrogen, deuterium, halogen, -CN, -OR 100 , -SR 100 , -S(O)R 100 , -S(O) 2 R 100 , -N(R 100 ) 2 , -P(O)(OR 100 ) 2 , -P(O)[N(R 100 ) 2 ](OR 100 ), -P(O)[N(R 100 ) 2 ] 2 , -Si(OH) 2 (R 100 )-, -Si(OH)(R 100 ) 2 -, -Si(R 100 ) 3 -, or optionally substituted C1-C4 alkyl; or
R 701和X 101或者X 301与其所连接的原子一起形成5-7元饱和的或者部分不饱和的碳环或者含有1-3个选自硼、N、O、Si或者S杂原子的杂环； R 701 and X 101 or X 301 together with the atoms to which they are attached form a 5-7 membered saturated or partially unsaturated carbocyclic ring or a heterocyclic ring containing 1-3 heteroatoms selected from boron, N, O, Si or S ;
或者相同碳上的两个R 701与其所连接的原子一起形成3-6元环或者含有1-2个选自硼、N、O、Si或者S杂原子的4-7元杂环； Or two R 701 on the same carbon together with the atoms to which they are attached form a 3-6 membered ring or a 4-7 membered heterocycle containing 1-2 heteroatoms selected from boron, N, O, Si or S;
或者相邻碳上的两个R 701与其所连接原子一起形成3-7元饱和的或者部分不饱和的碳环或者含有1-3个选自硼、N、O、Si或者S杂原子的杂环，或者形成饱和的或者部分不饱和的含有1-3个选自硼、N、O、Si或者S杂原子的7-13元桥杂环或螺杂环； Or two R 701 on adjacent carbons together with their attached atoms form a 3-7 membered saturated or partially unsaturated carbocyclic ring or a heteroatom containing 1-3 heteroatoms selected from boron, N, O, Si or S ring, or form a saturated or partially unsaturated 7-13 membered bridged heterocycle or spiro heterocycle containing 1-3 heteroatoms selected from boron, N, O, Si or S;
环D各自独立的为含有1-4个选自N、O或者S杂原子的6-元杂芳基、苯基、5-7元饱和或部分不饱和的环烷基、含有1-3个选自N、O、S杂原子的5-7元饱和或部分不饱和的杂环烷基、或者含有1-4个选自N、O、S杂原子的5元杂芳基；Ring D is each independently a 6-membered heteroaryl, phenyl, 5-7 membered saturated or partially unsaturated cycloalkyl containing 1-4 heteroatoms selected from N, O or S heteroatoms, containing 1-3 5-7-membered saturated or partially unsaturated heterocycloalkyl selected from N, O, S heteroatoms, or 5-membered heteroaryl containing 1-4 heteroatoms selected from N, O, S;
L 101为键或C 1-C 4亚烷基，所述C 1-C 4亚烷基中1个或2亚甲基任选被选自-O-、-C(O)-、-C(S)-、-C(R 100) 2-、-CH(R 100)-、-C(F) 2-、-N(R 100)-、-S-、-S(O) 2-或者-CH＝CH-的基团替代； L 101 is a bond or a C 1 -C 4 alkylene group, and 1 or 2 methylene groups in the C 1 -C 4 alkylene group are optionally selected from -O-, -C(O)-, -C (S)-, -C(R 100 ) 2 -, -CH(R 100 )-, -C(F) 2 -, -N(R 100 )-, -S-, -S(O) 2 - or -CH=CH- group substitution;
n”为0、1、2、3或4；n" is 0, 1, 2, 3 or 4;
q”为0、1、2、3或4。q" is 0, 1, 2, 3 or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E6、E6a、E6b、E6c、E6d、E6e、E6f、E6g、E6h或者E6i：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E6, E6a, E6b, E6c, E6d, E6e, E6f, E6g, E6h or E6i:
Figure PCTCN2022088560-appb-000327
Figure PCTCN2022088560-appb-000327
Figure PCTCN2022088560-appb-000328
Figure PCTCN2022088560-appb-000328
其中所述E6、E6a、E6b、E6c、E6d、E6e、E6f、E6g、E6h或者E6i中：Wherein said E6, E6a, E6b, E6c, E6d, E6e, E6f, E6g, E6h or E6i:
Figure PCTCN2022088560-appb-000329
为
Figure PCTCN2022088560-appb-000330
Figure PCTCN2022088560-appb-000329
for
Figure PCTCN2022088560-appb-000330
Y为键、Y 1、O、NH、NR 2、C(O)O、C(O)NR 2'、Y 1-O、Y 1-NH、Y 1-NR 2、Y 1-C(O)、Y1-C(O)O、Y 1-OC(O)、Y 1-C(O)NR 2'或Y 1-NR 2'C(O)，其中Y 1是C 1-C 6亚烷基、C 2-C 6烯基或C 2-C 6烷炔基； Y is a bond, Y 1 , O, NH, NR 2 , C(O)O, C(O)NR 2 ', Y 1 -O, Y 1 -NH, Y 1 -NR 2 , Y 1 -C(O ), Y1-C(O)O, Y1 -OC(O), Y1 -C(O)NR2' or Y1 - NR2'C (O), wherein Y1 is C1 - C6 sub alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl;
X为C(O)或C(R 3) 2； X is C(O) or C(R 3 ) 2 ;
X 1-X 2为C(R 3)＝N或C(R 3) 2-C(R 3) 2； X 1 -X 2 is C(R 3 )=N or C(R 3 ) 2 -C(R 3 ) 2 ;
每个R 1独立地是卤素、硝基、NH 2、OH、C(O)OH、C 1-C 6烷基或C 1-C 6烷氧基； each R 1 is independently halogen, nitro, NH 2 , OH, C(O)OH, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
R 2是C 1-C 6烷基、C 2-C 6烯基、C 3-C 8环烷基、3-8元杂环烷基或C(O)-3-8元杂环烷基，且R 2可任选地被一个或多个卤素、N(R a) 2、NHC(O)R a、NHC(O)OR a、OR b、C 3-C 8环烷基、3-8元杂环烷基、C 6-C 10芳基、或5-10元杂芳基，其中C 3-C 8环烷基、3-8元杂环烷基、C 6-C 10芳基或5-10元杂芳基可任选地被一个或多个卤素、NH 2、CN、硝基、OH、C(O)OH、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6烷氧基或C 1-C 6卤代烷氧基取代； R 2 is C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl or C(O)-3-8 membered heterocycloalkyl , and R 2 can be optionally selected by one or more of halogen, N(R a ) 2 , NHC(O)R a , NHC(O)OR a , OR b , C 3 -C 8 cycloalkyl, 3- 8-membered heterocycloalkyl, C 6 -C 10 -membered aryl, or 5-10-membered heteroaryl, wherein C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, C 6 -C 10 -aryl or 5-10 membered heteroaryl can be optionally replaced by one or more halogen, NH2 , CN, nitro, OH, C(O)OH, C1 - C6 alkyl, C1 - C6 haloalkyl , C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy substituted;
R 2'为H、C 1-C 6烷基、C 2-C 6烯基、C 3-C 8环烷基或3-8-元杂杂环烷基，且当R 2'不是H时，可以任选地被一个或多个卤素、N(R a) 2、NHC(O)R a、NHC(O)OR a、OR b、C 3-C 8环烷基、3-8元杂环烷基、C 6-C 10芳基或5-10元杂芳基所取代，其中C 3-C 8环烷基、3-8元杂环烷基、C 6-C 10芳基或5-10元杂芳基可任选地被另一种或多种卤素、NH 2、CN、硝基、OH、C(O)OH、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6烷氧基或C 1-C 6卤代烷氧基取代； R 2 ′ is H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 3 -C 8 cycloalkyl or 3-8-membered heteroheterocycloalkyl, and when R 2 ′ is not H , which can be optionally replaced by one or more halogens, N(R a ) 2 , NHC(O)R a , NHC(O)OR a , OR b , C 3 -C 8 cycloalkyl, 3-8 membered hetero substituted by cycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl, wherein C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, C 6 -C 10 aryl or 5 -10 membered heteroaryl can be optionally substituted by another one or more halogen, NH2 , CN, nitro, OH, C(O)OH, C1 - C6 alkyl, C1 - C6 haloalkyl , C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy substituted;
每个R 3独立地是H或C 1-C 3烷基，所述C 1-C 3烷基任选地被C 6-C 10芳基或5-10元杂芳基取代； each R is independently H or C 1 -C 3 alkyl optionally substituted with C 6 -C 10 aryl or 5-10 membered heteroaryl ;
每个R 3'是独立的C 1-C 3烷基； each R 3 ' is an independent C 1 -C 3 alkyl;
每个R 4独立地为H或C 1-C 3烷基；或两个R 4与它们连接的碳原子一起形成C(O)、C 3-C 6环烷基或含有1或2个选自N和O的杂原子的4-,5-或6-元杂环烷基； Each R 4 is independently H or C 1 -C 3 alkyl; or two R 4 together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl or contain 1 or 2 optional 4-, 5- or 6-membered heterocycloalkyl from heteroatoms of N and O;
R 5是H、C 1-C 3烷基、F或Cl； R 5 is H, C 1 -C 3 alkyl, F or Cl;
每个R a独立地是H或C 1-C 6烷基； each R is independently H or C 1 -C 6 alkyl ;
R b是H或甲苯磺酰基； R b is H or tosyl;
t是0或l；t is 0 or 1;
m是0、1、2或3；m is 0, 1, 2 or 3;
n是0、1或2。n is 0, 1 or 2.
环A、X、X 1、X 2、Y 100、R 1、R 3、R 3′、R 4、R 5、t、m和n如WO2017/007612和US2018/0134684中所定义，并通过全文引用并入此文。 Rings A, X, X 1 , X 2 , Y 100 , R 1 , R 3 , R 3′ , R 4 , R 5 , t, m and n are as defined in WO2017/007612 and US2018/0134684, and through in their entirety Incorporated herein by reference.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E7、E7b、E7c、E7d或者E7e：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E7, E7b, E7c, E7d or E7e:
Figure PCTCN2022088560-appb-000331
Figure PCTCN2022088560-appb-000331
其中所述E7、E7b、E7c、E7d和E7e中：Wherein said E7, E7b, E7c, E7d and E7e:
W为CH 2、CR aR b、C(S)、C(O)或SO 2； W is CH 2 , CR a R b , C(S), C(O) or SO 2 ;
X为H 2、CH 2、O或S； X is H 2 , CH 2 , O or S;
Y为NH、N-烷基、N-芳基、N-杂芳基、N-环烷基、N-杂环烷基、O或S；Y is NH, N-alkyl, N-aryl, N-heteroaryl, N-cycloalkyl, N-heterocycloalkyl, O or S;
Z为H 2、CH 2、O或者S，且E7c中，Z不能同时为H 2； Z is H 2 , CH 2 , O or S, and in E7c, Z cannot be H 2 at the same time;
G和G′各自独立的选自氢、C 1-C 6烷基、OH、任选被R ′取代的-CH 2-杂环烷基、任选被R ′取代的-CH 2-苯基； G and G' are each independently selected from hydrogen, C1 - C6 alkyl, OH, -CH2 -heterocycloalkyl optionally substituted with R ' , -CH2 -phenyl optionally substituted with R ' ;
Q 1、Q 2、Q 3、Q 4各自独立的为碳、氮或者氮氧化物； Q 1 , Q 2 , Q 3 and Q 4 are each independently carbon, nitrogen or nitrogen oxides;
A为氢、C 1-C 6烷基、环烷基或卤素； A is hydrogen, C 1 -C 6 alkyl, cycloalkyl or halogen;
R、R a和R b各自独立的选自氢、羟基、卤素、-NH 2、-N(C 1-C 6烷基) 1-2、C 1-C 6烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、-CONR ′R″、-OR ′、-NR ′R″、-SR ′、-SO 2R ′、-SO 2NR ′R″、-CR ′R″、-CR ′NR ′R″、芳基、杂芳基、C 3-C 8环烷基、3-8元杂环烷基、-P(O)(OR ′)R″、-P(O)R ′R″、-OP(O)(OR ′)R″、-Cl、-F、-Br、-I、-CF 3、-CN、-NR ′SO 2NR ′R″、-NR ′C(O)NR ′R″、-C(O)NR ′C(O)R″、-NR ′C(＝N-CN)NR ′R″、-C(＝N-CN)NR ′R″、-NR ′C(＝N-CN)R″、-NR ′C(＝C-NO 2)NR ′R″、-SO 2NR ′COR″、-NO 2、-COR ′、-C(C＝N-OR ′)R″、-CR ′＝CR ′R″、-CCR ′、-S(C＝O)(C＝N-R ′)R″、-SF 5或-OCF 3； R, R a and R b are each independently selected from hydrogen, hydroxy, halogen, -NH 2 , -N(C 1 -C 6 alkyl) 1-2 , C 1 -C 6 alkyl, C 1 -C 6 Alkoxy, C 1 -C 6 haloalkyl, -CONR ' R", -OR ' , -NR ' R", -SR ' , -SO 2 R ' , -SO 2 NR ' R", -CR ' R ", -CR ' NR ' R ", aryl, heteroaryl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, -P(O)(OR ' )R", -P( O) R'R", -OP(O)(OR' ) R", -Cl, -F, -Br, -I, -CF3 , -CN, -NR'SO2NR'R " , -NR ' C(O)NR'R " ,-C(O) NR'C (O)R " ,- NR'C (=N-CN)NR'R " ,-C(=N-CN)NR'R ", -NR'C (=N-CN)R", -NR'C (=C-NO2 ) NR'R", -SO2NR'COR " , -NO2 , -COR ' , -C ( C=N-OR ' )R", -CR ' =CR'R", -CCR' , -S(C=O)(C=NR ' )R", -SF5 or -OCF3 ;
R ′和R″各自独立的选自键、氢、C 1-C 6烷基、环烷基、芳基、杂芳基或杂环烷基； R ' and R" are each independently selected from bond, hydrogen, C1 - C6 alkyl, cycloalkyl, aryl, heteroaryl or heterocycloalkyl;
n″为1-4的整数；n" is an integer from 1 to 4;
-----为键，其可为R立体异构体、S立体异构体或非立体异构体。----- is a bond, which may be an R stereoisomer, an S stereoisomer, or a non-stereoisomer.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is:
Figure PCTCN2022088560-appb-000332
Figure PCTCN2022088560-appb-000332
Figure PCTCN2022088560-appb-000333
Figure PCTCN2022088560-appb-000333
Figure PCTCN2022088560-appb-000334
Figure PCTCN2022088560-appb-000334
Figure PCTCN2022088560-appb-000335
Figure PCTCN2022088560-appb-000335
Figure PCTCN2022088560-appb-000336
Figure PCTCN2022088560-appb-000336
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E8、E8a、E8b、E8c、E8d、E8e、E8f、E8g、E8h、E8i、E8j、E8k、E8l、E8m、E8n、E8o、E8p、E8q、E8s、E8t、E8u、E8v、E8w、E8x、E8y、E8z、E8aa、E8bb或E8cc：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment, E is E8, E8a, E8b, E8c, E8d, E8e, E8f, E8g, E8h, E8i, E8j, E8k, E8l, E8m, E8n, E8o, E8p, E8q, E8s, E8t, E8u , E8v, E8w, E8x, E8y, E8z, E8aa, E8bb or E8cc:
Figure PCTCN2022088560-appb-000337
Figure PCTCN2022088560-appb-000337
Figure PCTCN2022088560-appb-000338
Figure PCTCN2022088560-appb-000338
Figure PCTCN2022088560-appb-000339
Figure PCTCN2022088560-appb-000339
其中所述E8、E8a、E8b、E8c、E8d、E8e、E8f、E8g、E8h、E8i、E8j、E8k、E8l、E8m、E8n、E8o、E8p、E8q、E8s、E8t、E8u、E8v、E8w、E8x、E8y、E8z、E8aa、E8bb或E8cc中：wherein the E8, E8a, E8b, E8c, E8d, E8e, E8f, E8g, E8h, E8i, E8j, E8k, E8l, E8m, E8n, E8o, E8p, E8q, E8s, E8t, E8u, E8v, E8w, E8x , E8y, E8z, E8aa, E8bb or E8cc:
W各自独立的选自CH 2、CHR、C(O)或SO 2； Each W is independently selected from CH 2 , CHR, C(O) or SO 2 ;
Q 1、Q 2、Q 3、Q 4、Q 5各自独立的为碳、N、或者被R’取代的N，或者氮氧化物； Q 1 , Q 2 , Q 3 , Q 4 , Q 5 are each independently carbon, N, or N substituted by R', or nitrogen oxides;
R 1不存在、或者为氢、羟基、氰基、C 1-C 3烷基或者C(O)； R 1 is absent or is hydrogen, hydroxyl, cyano, C 1 -C 3 alkyl or C(O);
R 2不存在、或者为氢、羟基、氰基、C 1-C 3烷基、CHF 2、CF 3、CHO或者C(O)NH 2； R 2 is absent, or is hydrogen, hydroxyl, cyano, C 1 -C 3 alkyl, CHF 2 , CF 3 , CHO or C(O)NH 2 ;
R 3选自氢、烷基(如：C 1-C 6烷基或者C 1-C 3烷基)、任选被取代的烷基(如：C 1-C 6烷基或者C 1-C 3烷基)、烷氧基(如：C 1-C 6烷氧基或者C 1-C 3烷氧基)、任选被取代的烷氧基(如：C 1-C 6烷氧基或者C 1-C 3烷氧基)； R 3 is selected from hydrogen, alkyl (eg: C 1 -C 6 alkyl or C 1 -C 3 alkyl), optionally substituted alkyl (eg: C 1 -C 6 alkyl or C 1 -C 3 alkyl), alkoxy (such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy), optionally substituted alkoxy (such as: C 1 -C 6 alkoxy or C 1 -C 3 alkoxy);
R 4选自氢、烷基或者任选被取代的烷基； R4 is selected from hydrogen, alkyl or optionally substituted alkyl;
R 5或者R 6各自独立的选自氢、卤素、C(O)R’、氰基、羟基、CF 3； R 5 or R 6 are each independently selected from hydrogen, halogen, C(O)R', cyano, hydroxyl, CF 3 ;
X为碳、氮或者C(O)；X is carbon, nitrogen or C(O);
X 1为碳、氮或者C(O)； X 1 is carbon, nitrogen or C(O);
R’选自氢、卤素、胺、烷基(如：C 1-C 3烷基)、任选取代的烷基(如：C 1-C 3烷基)、烷氧基(如：C 1-C 3烷氧基)、任选取代的烷氧基(如：C 1-C 3烷氧基)、NR 2R 3、C(O)OR 2、任选取代的苯基； R' is selected from hydrogen, halogen, amine, alkyl (eg: C 1 -C 3 alkyl), optionally substituted alkyl (eg: C 1 -C 3 alkyl), alkoxy (eg: C 1 -C 3 alkoxy), optionally substituted alkoxy (eg: C 1 -C 3 alkoxy), NR 2 R 3 , C(O)OR 2 , optionally substituted phenyl;
R为H、OH、低级烷基、低级烷氧基、氰基、卤代低级烷氧基或卤代低级烷基；R is H, OH, lower alkyl, lower alkoxy, cyano, halogenated lower alkoxy or halogenated lower alkyl;
n为0、1、2、3或者4；n is 0, 1, 2, 3 or 4;
Figure PCTCN2022088560-appb-000340
为单键或者双键。
Figure PCTCN2022088560-appb-000340
single or double bond.
本发明式Ⅰ化合物、和/或其立体异构体、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E9a、E9b、E9c、E9d、E9e、E9f、E9g、E9h、E9i、E9j、E9k、E9l、E9m、E9n、E9o、E9p、E9q、E9r或E9s：In a preferred embodiment of the compound of formula I, and/or its stereoisomers, hydrates, solvates, prodrugs and/or pharmaceutically acceptable salts thereof, E is E9a, E9b, E9c, E9d, E9e, E9f, E9g, E9h, E9i, E9j, E9k, E9l, E9m, E9n, E9o, E9p, E9q, E9r, or E9s:
Figure PCTCN2022088560-appb-000341
Figure PCTCN2022088560-appb-000341
其中所述E9a、E9b、E9c、E9d、E9e、E9f、E9g、E9h、E9i、E9j、E9k、E9l、E9m、E9n、E9o、E9p、E9q、E9r或E9s中：wherein said E9a, E9b, E9c, E9d, E9e, E9f, E9g, E9h, E9i, E9j, E9k, E9l, E9m, E9n, E9o, E9p, E9q, E9r or E9s:
W独立地选自CH 2、CHR、C＝O、SO 2、NH和N-烷基； W is independently selected from CH2 , CHR, C=O, SO2, NH and N - alkyl;
R 1选自H、CN、C 1-C 3烷基； R 1 is selected from H, CN, C 1 -C 3 alkyl;
R 2是H或C 1-C 3烷基； R 2 is H or C 1 -C 3 alkyl;
R 4是甲基或乙基； R 4 is methyl or ethyl;
R 5是H或卤素； R 5 is H or halogen;
R 6是H或卤素； R 6 is H or halogen;
R是H；R is H;
R’是H；R' is H;
Q 1和Q 2各自独立地是被独立地选自H或C 1-C 3烷基的基团取代的C或N； Q 1 and Q 2 are each independently C or N substituted with a group independently selected from H or C 1 -C 3 alkyl;
Figure PCTCN2022088560-appb-000342
是单键或双键。
Figure PCTCN2022088560-appb-000342
is a single or double bond.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E10、E10a或E10b：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E10, E10a or E10b:
Figure PCTCN2022088560-appb-000343
Figure PCTCN2022088560-appb-000343
其中所述E10、E10a或E10b中：所述X A为C(O)或者C(R 3A) 2； wherein in the E10, E10a or E10b: the X A is C(O) or C(R 3A ) 2 ;
Z为NR 3A或者CR 3A； Z is NR 3A or CR 3A ;
每个R 1A各自独立的为卤素、羟基、-C 1-C 6烷基或者C 1-C 6烷氧基； Each R 1A is independently halogen, hydroxy, -C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
每个R 3A各自独立的为氢或者C 1-C 3烷基； Each R 3A is independently hydrogen or C 1 -C 3 alkyl;
R 3’各自独立的为C 1-C 3烷基； R 3' is each independently C 1 -C 3 alkyl;
每个R 4A各自独立的为氢或者C 1-C 3烷基，或者两个R 4A与其所连接的碳原子一起形成C(O)、C3-C6环烷基、或者一起形成含有1个或者2个选自N或者O杂原子的3元、4元、5元或者6元杂环烷基； Each R 4A is independently hydrogen or C 1 -C 3 alkyl, or two R 4A together with the carbon atom to which they are attached form C(O), C3-C6 cycloalkyl, or together form a C(O), C3-C6 cycloalkyl group containing 1 or 2 3-membered, 4-membered, 5-membered or 6-membered heterocycloalkyl selected from N or O heteroatoms;
R 5A选自氢、C 1-C 3烷基或者卤素； R 5A is selected from hydrogen, C 1 -C 3 alkyl or halogen;
每个R 6A各自独立的为氢或者C 1-C 3烷基，或者两个R 6A与其所连接的碳原子一起形成C(O)、C 3-C 6环烷基、或者一起形成含有1个或者2个选自N或者O杂原子的3元、4元、5元或者6元杂环烷基； Each R 6A is independently hydrogen or C 1 -C 3 alkyl, or two R 6A together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl, or together form a C(O), C 3 -C 6 cycloalkyl group containing 1 one or two 3-, 4-, 5- or 6-membered heterocycloalkyls selected from N or O heteroatoms;
m为0、1、2或者3；m is 0, 1, 2 or 3;
n为0、1或者2；n is 0, 1 or 2;
a1为0或者1。a1 is 0 or 1.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E11：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E11:
Figure PCTCN2022088560-appb-000344
Figure PCTCN2022088560-appb-000344
其中所述E11中：-X 1-X 2-为-C(R 3A)＝N-或者-C(R 3A) 2-C(R 3A) 2-； Wherein in said E11: -X 1 -X 2 - is -C(R 3A )=N- or -C(R 3A ) 2 -C(R 3A ) 2 -;
每个R 1A各自独立的为卤素、羟基、C 1-C 6烷基或者C 1-C 6烷氧基； Each R 1A is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
R 3A为氢或C 1-C 3烷基； R 3A is hydrogen or C 1 -C 3 alkyl;
R 3’各自独立的为C 1-C 3烷基； R 3' is each independently C 1 -C 3 alkyl;
R 4A为氢、或者C 1-C 3烷基；或者两个R 4A与其所连接的碳原子一起形成C(O)、C 3-C 6环烷基、或者一起形成含有1个或者2个选自N或者O杂原子的4元、5元或者6元杂环烷基； R 4A is hydrogen, or C 1 -C 3 alkyl; or two R 4A together with the carbon atom to which they are attached form C(O), C 3 -C 6 cycloalkyl, or together form a cycloalkyl containing 1 or 2 4-membered, 5-membered or 6-membered heterocycloalkyl selected from N or O heteroatoms;
m为0、1、2或者3；m is 0, 1, 2 or 3;
n为0、1或者2；n is 0, 1 or 2;
a1为0或者1。a1 is 0 or 1.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E12：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E12:
Figure PCTCN2022088560-appb-000345
Figure PCTCN2022088560-appb-000345
其中所述E12中：Among the E12:
每个R 2’各自独立的为卤素、羟基、C 1-C 6烷基或者C 1-C 6烷氧基； Each R 2' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
每个R 4’各自独立的为卤素、羟基、C 1-C 6烷基或者C 1-C 6烷氧基； Each R 4' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
每个R 5’各自独立的为卤素、羟基、C 1-C 6烷基或者C 1-C 6烷氧基； Each R 5' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
n1为0、1、2、3、4、5或者6；n1 is 0, 1, 2, 3, 4, 5 or 6;
n2为0、1、2、3或者4；n2 is 0, 1, 2, 3 or 4;
n3为0、1或者2。n3 is 0, 1 or 2.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E13：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E13:
Figure PCTCN2022088560-appb-000346
Figure PCTCN2022088560-appb-000346
Figure PCTCN2022088560-appb-000347
Figure PCTCN2022088560-appb-000347
其中所述E13中：Among the E13:
R 3A为氢、或者C1-C3烷基； R 3A is hydrogen, or C1-C3 alkyl;
每个R 3’为C 1-C 3烷基； each R 3' is C 1 -C 3 alkyl;
每个R 6’各自独立的为卤素、羟基、C 1-C 6烷基或者C 1-C 6烷氧基； Each R 6' is independently halogen, hydroxy, C 1 -C 6 alkyl or C 1 -C 6 alkoxy;
n1为0、1、2、3、4或者5；n1 is 0, 1, 2, 3, 4 or 5;
m1为0、1、2、3、4或者5。m1 is 0, 1, 2, 3, 4, or 5.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E14、E14a、E14b、E14c、E14d或E14e：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E14, E14a, E14b, E14c, E14d or E14e:
Figure PCTCN2022088560-appb-000348
Figure PCTCN2022088560-appb-000348
其中所述E14、E14a、E14b、E14c、E14d和E14e中，wherein among the E14, E14a, E14b, E14c, E14d and E14e,
Ar为芳基、环烷基、杂环烷基或者杂芳基；Ar is aryl, cycloalkyl, heterocycloalkyl or heteroaryl;
L不存在或者为-SO 2、-SO 2R’、SO 2R'R”、-SO 2NR'R”、-SO 2NR'R”C(＝O)、-NR'SO 2R”、-R'SO 2NR'R”'、-C(＝O)；、-C(＝O)R'、-OC(＝O)R'、-C(＝O)NR'R”、-NR'C(＝O)R”、-NR'C(＝O)、R”C(＝O)、-OR'；、-NR'R”、-SR'、-N 3-C(＝O)OR'、-O(CR'R”) rC(＝O)R'、-O(CR'R”) rNR”C(＝O)R'、-O(CR'R”) rNR”SO 2R'、-OC(＝O)NR'R'、-NR'C(＝O)OR”或者任取代的C 1-C 6烷基； L is absent or is -SO2 , -SO2R ', SO2R'R ", -SO2NR'R ", -SO2NR'R "C(=O), -NR'SO2R ",-R'SO 2 NR'R"',-C(=O);,-C(=O)R',-OC(=O)R',-C(=O)NR'R",- NR'C(=O)R", -NR'C(=O), R"C(=O), -OR';, -NR'R", -SR', -N 3 -C(=O )OR', -O(CR'R") r C(=O)R', -O(CR'R") r NR"C(=O)R',-O(CR'R") r NR "SO 2 R', -OC(=O)NR'R', -NR'C(=O)OR" or optionally substituted C 1 -C 6 alkyl;
R'、R”、R”'各自独立的选自H、取代或未取代的烷基、取代或未取代的烯基、取代或未取代的醚基、取代或未取代的环烷基、取代或未取代的杂环烷基、取代或未取代的环烯基、取代或未取代的芳基、取代 或未取代的杂芳基、取代或未取代的芳基烷基、取代或未取代的杂烷基、取代或未取代的烷基化酰基芳基、或取代或未取代的胺；r是1到6的整数；R', R", R"' are each independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted ether, substituted or unsubstituted cycloalkyl, substituted or unsubstituted or unsubstituted heterocycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted Heteroalkyl, substituted or unsubstituted alkylated acylaryl, or substituted or unsubstituted amine; r is an integer from 1 to 6;
R 1、R 2、R 3各自独立的选自H、卤素、羟基、叠氮化物、烷氧基、巯基、亚氨基、氨基、膦酸盐、磷酸盐、羰基、羧基、氰基、甲硅烷基、醚、烷硫基、磺酰基、磺酰氨基、酮、醛、取代或未取代的胺、取代或未取代的酰胺、硝基、酯、吗啉基、二氧戊烷、取代或未取代的烷基、取代或未取代的卤代烷基、取代或未取代的环烷基、取代或未取代的杂环烷基、取代或未取代的环烯基、取代或未取代的芳基、取代或未取代的杂芳基、取代或未取代的芳基烷基、替代或者未取代的杂芳基烷基、取代或未取代的烷基杂芳基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、取代或未取代的杂环烷基、或者它们的组合； R 1 , R 2 , R 3 are each independently selected from H, halogen, hydroxyl, azide, alkoxy, mercapto, imino, amino, phosphonate, phosphate, carbonyl, carboxyl, cyano, silane group, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, substituted or unsubstituted amine, substituted or unsubstituted amide, nitro, ester, morpholinyl, dioxolane, substituted or unsubstituted substituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted or unsubstituted heteroaryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted heteroarylalkyl, substituted or unsubstituted alkylheteroaryl, substituted or unsubstituted alkenyl, substituted or unsubstituted unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, or a combination thereof;
或者R 1、R 2结合形成5-7元杂环，且当R 1、R 2结合形成5-7元杂环时，Ar与5-7元杂环未形成并环，而是5-7元杂环的取代基； Or R 1 and R 2 combine to form a 5-7 membered heterocycle, and when R 1 and R 2 combine to form a 5-7 membered heterocycle, Ar and the 5-7 membered heterocycle do not form a combined ring, but a 5-7 membered heterocycle. Substituents of membered heterocycles;
R 4、R 5为氢、卤素、羟基、叠氮、醚、烷氧基、巯基、烷硫基、磺酰基、磺酰氨酰胺、酮、醛、酯、取代或未取代的烷基、取代或未取代的卤代烷基、取代或未取代的芳烷基、取代或未取代的烯酮基、未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、杂环基或者其组合； R 4 , R 5 are hydrogen, halogen, hydroxyl, azide, ether, alkoxy, mercapto, alkylthio, sulfonyl, sulfonamide, ketone, aldehyde, ester, substituted or unsubstituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenone, unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocycle base or a combination thereof;
R 8为氢、取代或未取代的烷基、取代或未取代的卤代烷基、取代或未取代的芳基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、杂环基、取代或未取代的芳基、取代或未取代的烷基芳基或其组合； R 8 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted haloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted alkylaryl, or a combination thereof;
Figure PCTCN2022088560-appb-000349
为单键或双键；
Figure PCTCN2022088560-appb-000349
is a single bond or a double bond;
x为0、1或2；x is 0, 1 or 2;
y为1到6的整数。y is an integer from 1 to 6.
在一些实施方案中，所述E14、E14a、E14b、E14c、E14d和E14e中，Ar、R 1、R 2、R 3、R 4、R 5、R 6、R 7、R 8、A、L、x、y和
Figure PCTCN2022088560-appb-000350
如WO2017/161119(其全文通过引用的方式并入本文中)中所定义和描述。 In some embodiments, among the E14, E14a, E14b, E14c, E14d and E14e, Ar, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , A, L , x, y and
Figure PCTCN2022088560-appb-000350
As defined and described in WO2017/161119, which is incorporated herein by reference in its entirety.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E15、E15a、E15b、E15c、E15d、E15e、E15f、E15g或E15h：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of E15, E15a, E15b, E15c, E15d, E15e, E15f, E15g or E15h:
Figure PCTCN2022088560-appb-000351
Figure PCTCN2022088560-appb-000351
Figure PCTCN2022088560-appb-000352
Figure PCTCN2022088560-appb-000352
其中所述E15、E15a、E15b、E15c、E15d、E15e、E15f、E15g和E15h中：wherein said E15, E15a, E15b, E15c, E15d, E15e, E15f, E15g and E15h:
环B为芳基、杂芳基、环烷基、杂环烷基；Ring B is aryl, heteroaryl, cycloalkyl, heterocycloalkyl;
L 101为键或C 1-C 6烷基； L 101 is a bond or C 1 -C 6 alkyl;
A为C、S、取代或未取代的C 1-C 8烷基或其组合； A is C, S, substituted or unsubstituted C 1 -C 8 alkyl or a combination thereof;
G 100为C、S、N、取代或为取代的C 1-C 8烷基或其组合； G 100 is C, S, N, substituted or substituted C 1 -C 8 alkyl or a combination thereof;
R 101、R 201和R 301分别选自氢、卤素、羟基、叠氮化物、烷氧基、巯基、亚氨基、酰氨基、膦酸酯、次膦酸酯、羰基、羧基、氰基、甲硅烷基、醚基、烷硫基、磺酰基、磺酰氨基、酮、醛、取代或未取代的胺、取代或未取代的酰胺、硝基、酯、吗啉代、二氧戊环、取代或未取代的烷基、取代或未取代的烷基卤化物、取代或未取代的芳烷基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、取代或未取代的环烷基；取代或未取代的杂环烷基；取代或未取代的环烯基、取代或未取代的芳基、取代或未取代的杂芳基、取代或未取代的芳烷基、取代或未取代的杂烷基、取代或未取代的烷基杂芳基、及其组合；或其中R 101和R 201结合形成5-7元杂环烷基；其中当R 101和R 201结合形成5-7元杂环时，环B任选不与5-7元杂环稠合，但是是5-7元杂环的取代基； R 101 , R 201 and R 301 are independently selected from hydrogen, halogen, hydroxyl, azide, alkoxy, mercapto, imino, amido, phosphonate, phosphinate, carbonyl, carboxyl, cyano, methyl Silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, substituted or unsubstituted amine, substituted or unsubstituted amide, nitro, ester, morpholino, dioxolane, substituted or unsubstituted alkyl, substituted or unsubstituted alkyl halide, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl , substituted or unsubstituted cycloalkyl; substituted or unsubstituted heterocycloalkyl; substituted or unsubstituted cycloalkenyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted alkyl heteroaryl, and combinations thereof; or wherein R 101 and R 201 combine to form a 5-7 membered heterocycloalkyl; wherein when R When 101 and R 201 combine to form a 5-7-membered heterocycle, ring B is optionally not condensed with the 5-7-membered heterocycle, but is a substituent of the 5-7-membered heterocycle;
R 401和R 501分别选自氢、卤素、羟基、叠氮化物、醚、烷氧基、巯基、烷硫基、磺酰基、磺酰氨基、酮、醛、酯、取代或未取代的烷基、取代或未取代的烷基卤化物、取代或未取代的芳烷基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、杂环烷基及其组合； R 401 and R 501 are independently selected from hydrogen, halogen, hydroxyl, azide, ether, alkoxy, mercapto, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, substituted or unsubstituted alkyl , substituted or unsubstituted alkyl halides, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted cycloalkyl, heterocycloalkyl and its combination;
R 601和R 701各自独立的为氧代、氢、C 1-C 8烷基、或R 601和R 701一起结合形成氧代； R 601 and R 701 are each independently oxo, hydrogen, C 1 -C 8 alkyl, or R 601 and R 701 combine together to form oxo;
R 801选自氢、取代或未取代的烷基、取代或未取代的烷基卤化物、取代或未取代的芳烷基、取代或未取代的烯基、取代或未取代的炔基、取代或未取代的环烷基、杂环烷基、取代或未取代的芳基、取代或未取代的烷芳基、及其组合； R 801 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyl halide, substituted or unsubstituted aralkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted or unsubstituted cycloalkyl, heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkaryl, and combinations thereof;
x”、y”各自独立的为0、1或2；x" and y" are independently 0, 1 or 2;
Figure PCTCN2022088560-appb-000353
为单键或双键；
Figure PCTCN2022088560-appb-000353
is a single bond or a double bond;
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E16、E16a或E16b：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E16, E16a or E16b:
Figure PCTCN2022088560-appb-000354
Figure PCTCN2022088560-appb-000354
Figure PCTCN2022088560-appb-000355
Figure PCTCN2022088560-appb-000355
其中所述E16、E16a和E16b中：wherein said E16, E16a and E16b:
W 101为CR 601R 701、C(O)、C(S)、C＝CH 2、SO 2、S(O)、P(O)O烷基、P(O)NH烷基、P(O)N(烷基) 2、P(O)烷基、P(O)OH、P(O)NH 2； W 101 is CR 601 R 701 , C(O), C(S), C=CH 2 , SO 2 , S(O), P(O)O alkyl, P(O)NH alkyl, P(O ) N(alkyl) 2 , P(O) alkyl, P(O)OH, P(O)NH 2 ;
W 201是CR 801R 901、C(O)、C(S)、C＝CH 2、SO 2、S(O)、P(O)O烷基、P(O)NH烷基、P(O)N(烷基) 2、P(O)烷基、P(O)OH、P(O)NH 2； W 201 is CR 801 R 901 , C(O), C(S), C=CH 2 , SO 2 , S(O), P(O)O alkyl, P(O)NH alkyl, P(O ) N(alkyl) 2 , P(O) alkyl, P(O)OH, P(O)NH 2 ;
X 100独立地选自NH、NR 301、CH 2、CHR 301、C(R 301) 2、O或S； X 100 is independently selected from NH, NR 301 , CH 2 , CHR 301 , C(R 301 ) 2 , O or S;
n”为0、1、2或3；n" is 0, 1, 2 or 3;
Figure PCTCN2022088560-appb-000356
为单键或双键；其中当
Figure PCTCN2022088560-appb-000357
为单键时，n”为0、1、2或3；当
Figure PCTCN2022088560-appb-000358
为双键时，n”为0、1或2；
Figure PCTCN2022088560-appb-000356
is a single bond or a double bond; where when
Figure PCTCN2022088560-appb-000357
When it is a single bond, n" is 0, 1, 2 or 3; when
Figure PCTCN2022088560-appb-000358
When it is a double bond, n" is 0, 1 or 2;
R 101选自： R 101 is selected from:
Figure PCTCN2022088560-appb-000359
Figure PCTCN2022088560-appb-000359
Figure PCTCN2022088560-appb-000360
Figure PCTCN2022088560-appb-000360
或者R 101*； or R 101* ;
R 201为烷基、氢、杂烷基、芳基、杂芳基或杂环烷基； R 201 is alkyl, hydrogen, heteroalkyl, aryl, heteroaryl or heterocycloalkyl;
或R 101和R 201结合形成4、5、6、7、8、9或10元杂环烷基或杂芳基，所述杂环烷基或杂芳基任选的被一个或多个选自R 501、R 120的取代基取代； Or R 101 and R 201 combine to form a 4, 5, 6, 7, 8, 9 or 10-membered heterocycloalkyl or heteroaryl, which is optionally selected by one or more Substituted from the substituents of R 501 and R 120 ;
R 101*选自： R 101* is selected from:
Figure PCTCN2022088560-appb-000361
Figure PCTCN2022088560-appb-000361
R 301选自：烷基、-C(O)H、C(O)OH、-C(O)烷基、-C(O)O烷基、烯基、炔基、芳基、杂芳基或杂烷基； R 301 is selected from: alkyl, -C(O)H, C(O)OH, -C(O) alkyl, -C(O)O alkyl, alkenyl, alkynyl, aryl, heteroaryl or heteroalkyl;
R 401选自烷基、烯基、炔基、卤素、羟基、烷氧基、叠氮基、氨基、氰基、-NH(烷基)、-N(烷基) 2、-NHS(O) 2(烷基)、-N(烷基)SO 2烷基、-NHSO 2(芳基、杂芳基或杂环烷基)、-N(烷基)SO 2(芳基、杂芳基或杂环烷基)、-NHSO 2(烯基)、-N(烷基)SO 2(烯基)、-NHSO 2(炔基)、-N(烷基)SO 2(炔基)或卤代烷基、芳基、杂芳基、杂烷基和环烷基； R 401 is selected from alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, cyano, -NH(alkyl), -N(alkyl) 2 , -NHS(O) 2 (alkyl), -N(alkyl)SO 2 alkyl, -NHSO 2 (aryl, heteroaryl or heterocycloalkyl), -N(alkyl)SO 2 (aryl, heteroaryl or Heterocycloalkyl), -NHSO 2 (alkenyl), -N(alkyl)SO 2 (alkenyl), -NHSO 2 (alkynyl), -N(alkyl)SO 2 (alkynyl), or haloalkyl , aryl, heteroaryl, heteroalkyl and cycloalkyl;
或两个R 401与其相连接的碳原子一起形成3、4、5或6元环； or two R 401 together with the carbon atoms to which they are attached form a 3, 4, 5 or 6 membered ring;
R 501和R 140各自独立的选自氢、烷基、烯基、炔基、卤素、羟基、烷氧基、叠氮基、氨基、氰基、-NH(烷基)、-N(烷基) 2、-NHS(O) 2(烷基)、-N(烷基)SO 2(烷基)、-NHSO 2(芳基、杂芳基或杂环烷基)、-N(烷基)SO 2(芳基、杂芳基或杂环烷基)、-NHSO 2(烯基)、-N(烷基)SO 2(烯基)、-NHSO 2(炔基)、-N(烷基)SO 2(炔基)或卤代烷基、芳基、杂芳基、杂烷基和环烷基； R 501 and R 140 are each independently selected from hydrogen, alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, cyano, -NH(alkyl), -N(alkyl ) 2 , -NHS(O) 2 (alkyl), -N(alkyl)SO 2 (alkyl), -NHSO 2 (aryl, heteroaryl or heterocycloalkyl), -N(alkyl) SO 2 (aryl, heteroaryl or heterocycloalkyl), -NHSO 2 (alkenyl), -N(alkyl)SO 2 (alkenyl), -NHSO 2 (alkynyl), -N(alkyl) ) SO 2 (alkynyl) or haloalkyl, aryl, heteroaryl, heteroalkyl and cycloalkyl;
或R 501独立地选自C(O)R 401、氰基、芳基、芳基氧基、杂环烷基、杂芳基、芳基烷基、烷氧基、羟基、O-芳烷基或环烷基； or R 501 is independently selected from C(O)R 401 , cyano, aryl, aryloxy, heterocycloalkyl, heteroaryl, arylalkyl, alkoxy, hydroxy, O-aralkyl or cycloalkyl;
R 601、R 701、R 801、R 901、R 1001、或R 110独立地选自氢、烷基、杂烷基、羟基、烷氧基、胺、-NH(烷基)和-N(烷基) 2； R 601 , R 701 , R 801 , R 901 , R 1001 , or R 110 are independently selected from hydrogen, alkyl, heteroalkyl, hydroxy, alkoxy, amine, -NH(alkyl), and -N(alk base) 2 ;
或R 601和R 701与它们连接的碳原子一起形成3、4、5或6-元螺碳环，或形成含有1或2个选自N、O杂原子的4、5、或6-元螺杂环； Either R 601 and R 701 together with the carbon atom to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle, or a 4, 5, or 6-membered ring containing 1 or 2 heteroatoms selected from N, O Spiroheterocycle;
或R 801和R 901与它们连接的碳原子一起形成3、4、5或6-元螺碳环；或形成含有1或2个选自N、O杂原子的4、5、或6-元螺杂环； Or R 801 and R 901 together with the carbon atoms to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle; or form a 4, 5, or 6-membered ring containing 1 or 2 heteroatoms selected from N, O Spiroheterocycle;
或R 1001和R 110与它们连接的碳原子一起形成3、4、5或6-元螺碳环；或形成含有1或2个选自N、O杂原子的4、5、或6-元螺杂环； or R 1001 and R 110 together with the carbon atom to which they are attached form a 3, 4, 5 or 6-membered spirocarbocycle; Spiroheterocycle;
或R 601和R 801一起形成1个或2个碳桥环； Or R 601 and R 801 together form 1 or 2 carbon bridged rings;
或R 601和R 1001一起形成1或2个碳桥环； Or R 601 and R 1001 together form 1 or 2 carbon bridged rings;
或R 801和R 1001一起形成1或2个碳桥环； Or R 801 and R 1001 together form 1 or 2 carbon bridged rings;
或R 601和R 140一起形成3、4、5或6个碳稠合环； or R 601 and R 140 together form a 3, 4, 5 or 6 carbon fused ring;
或R 140和R 1001一起形成3、4、5或6个碳稠合环； or R 140 and R 1001 together form a 3, 4, 5 or 6 carbon fused ring;
或R 801和R 140一起形成1或2个碳桥环； Or R 801 and R 140 together form 1 or 2 carbon bridged rings;
或R 401和R 140一起形成3、4、5或6个碳稠合环，其中所述R 501位于R 140α碳上，或者一起形成1、2、3或4个碳桥环，其中所述R 501不位于R 140α碳上； Or R 401 and R 140 together form a 3, 4, 5 or 6 carbon fused ring, wherein said R 501 is located on the alpha carbon of R 140 , or together form 1, 2, 3 or 4 carbon bridged rings, wherein said R 501 Said R 501 is not located on the R 140 alpha carbon;
R 120为L 100； R 120 is L 100 ;
R 170选自： R 170 is selected from:
Figure PCTCN2022088560-appb-000362
Figure PCTCN2022088560-appb-000362
Y 100选自N、CH或CR 101；其中0、1、2或3个Y 100为N； Y 100 is selected from N, CH or CR 101 ; wherein 0, 1, 2 or 3 Y 100 are N;
R 101独立地选自氢、烷基、烯基、炔基、卤代烷基、烷氧基、羟基、芳基、杂芳基、杂环烷基、芳烷基、杂芳烷基、杂环烷基、芳氧基、杂芳氧基、CN、-C(O)O烷基、-C(O)OH、NO 2、F、Cl、Br、I、CF 3、NH 2、NH(烷基)、N(烷基) 2、或杂烷基。 R 101 is independently selected from hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, hydroxy, aryl, heteroaryl, heterocycloalkyl, aralkyl, heteroaralkyl, heterocycloalkane group, aryloxy, heteroaryloxy, CN, -C(O)O alkyl, -C(O)OH, NO 2 , F, Cl, Br, I, CF 3 , NH 2 , NH(alkyl ), N(alkyl) 2 , or heteroalkyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E17、E17a、E17b或E17c：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E17, E17a, E17b or E17c:
Figure PCTCN2022088560-appb-000363
Figure PCTCN2022088560-appb-000363
其中所述E17、E17a、E17b和E17c中：wherein said E17, E17a, E17b and E17c:
W 1为CR 6R 7、C＝O、C＝S、C＝CH 2、SO 2、S(O)、P(O)O烷基、P(O)NH烷基、P(O)N(烷基) 2、P(O)烷基、P(O)OH或P(O)H 2； W 1 is CR 6 R 7 , C=O, C=S, C=CH 2 , SO 2 , S(O), P(O)O alkyl, P(O)NH alkyl, P(O)N (Alkyl) 2 , P(O)alkyl, P(O)OH or P(O)H 2 ;
W 2为CR 8R 9、C＝O、C＝S、C＝CH 2、SO 2、S(O)、P(O)O烷基、P(O)NH烷基、P(O)N(烷基) 2、P(O)烷基、P(O)OH或P(O)H 2； W 2 is CR 8 R 9 , C=O, C=S, C=CH 2 , SO 2 , S(O), P(O)O alkyl, P(O)NH alkyl, P(O)N (Alkyl) 2 , P(O)alkyl, P(O)OH or P(O)H 2 ;
X、X 1各自独立的选自NH、NR 3、CH 2、CHR 3、C(R 3) 2、O或S； X and X 1 are each independently selected from NH, NR 3 , CH 2 , CHR 3 , C(R 3 ) 2 , O or S;
n”为0、1、2或3；n" is 0, 1, 2 or 3;
Figure PCTCN2022088560-appb-000364
为单键或双键；且当
Figure PCTCN2022088560-appb-000365
为单键时，n”为0、1、2或3；
Figure PCTCN2022088560-appb-000366
为双键时，n”为0、1或2；
Figure PCTCN2022088560-appb-000364
is a single or double bond; and when
Figure PCTCN2022088560-appb-000365
When it is a single bond, n" is 0, 1, 2 or 3;
Figure PCTCN2022088560-appb-000366
When it is a double bond, n" is 0, 1 or 2;
R 1为
Figure PCTCN2022088560-appb-000367
或R 1*，其中，X为O或N，且当X为O氧时，R 2不存在； R1 is
Figure PCTCN2022088560-appb-000367
or R 1* , where X is O or N, and when X is O oxygen, R 2 is absent;
环A为苯基、5-6元杂芳基、3-6元环烷基或4-6元杂环烷基，所述苯基、5-6元杂芳基、3-6元环烷基或4-6元杂环烷基任选被R 12取代； Ring A is phenyl, 5-6 membered heteroaryl, 3-6 membered cycloalkyl or 4-6 membered heterocycloalkyl, said phenyl, 5-6 membered heteroaryl, 3-6 membered cycloalkane radical or 4-6 membered heterocycloalkyl optionally substituted by R 12 ;
环B为不存在、苯基或5-6元杂芳基，所述苯基或5-6元杂芳基任选被R 5或R 12取代； Ring B is absent, phenyl or 5-6 membered heteroaryl optionally substituted by R 5 or R 12 ;
R 2为烷基、H、脂肪族、杂脂肪族、芳基、杂芳基或杂环烷基； R 2 is alkyl, H, aliphatic, heteroaliphatic, aryl, heteroaryl or heterocycloalkyl;
R 1*为任取代的芳基、杂芳基、环烷基、杂环烷基、烷氨基、烷氧基、酯基、磺酰基或酰氨基； R 1* is optionally substituted aryl, heteroaryl, cycloalkyl, heterocycloalkyl, alkylamino, alkoxy, ester, sulfonyl or amido;
R 3为烷基、-C(O)H、-C(O)OH、-C(O)烷基、-C(O)O烷基、烯基或炔基； R is alkyl, -C(O)H, -C(O)OH, -C(O)alkyl, -C(O)Oalkyl, alkenyl or alkynyl;
R 4为烷基、烯基、炔基、卤素、羟基、烷氧基、叠氮基、氨基、-NH烷基、-N(烷基) 2、-NHSO 2烷基、-N(烷基)SO 2烷基、-NHSO 2芳基、-N(烷基)SO 2芳基、-NHSO 2烯基、-N(烷基)SO 2烯基、-NHSO 2炔基、-N(烷基)SO 2炔基或卤代烷烃； R 4 is alkyl, alkenyl, alkynyl, halogen, hydroxyl, alkoxy, azido, amino, -NH alkyl, -N(alkyl) 2 , -NHSO 2 alkyl, -N(alkyl )SO 2 alkyl, -NHSO 2 aryl, -N(alkyl) SO 2 aryl, -NHSO 2 alkenyl, -N(alkyl) SO 2 alkenyl, -NHSO 2 alkynyl, -N(alk base) SO 2 alkynyl or halogenated alkane;
或2个R 4与它们连接的C原子一起形成3元、4元、5元或6元环； or 2 R4 together with the C atoms to which they are attached form a 3-, 4-, 5- or 6-membered ring;
R 6、R 7、R 8、R 9、R 10和R 11独立地选自氢、烷基、脂肪族、杂脂族、羟基、烷氧基、胺、-NH(脂肪族，包括烷基)和-N(脂肪族，包括烷基) 2； R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are independently selected from hydrogen, alkyl, aliphatic, heteroaliphatic, hydroxy, alkoxy, amine, -NH (aliphatic, including alkyl ) and -N (aliphatic, including alkyl) 2 ;
或R 6、R 7与它们所键合的碳原子一起形成3、4、5或6元螺碳环，或4、5或6元螺环杂环，所述杂原子为1或2个N或O； Or R 6 , R 7 and the carbon atoms to which they are bonded together form a 3-, 4-, 5- or 6-membered spirocarbocyclic ring, or a 4-, 5- or 6-membered spirocyclic heterocyclic ring, and the heteroatom is 1 or 2 N or O;
或R 8、R 9与它们所键合的碳原子一起形成3、4、5或6元螺碳环，或4、5或6元螺环杂环，所述杂原子为1或2个N或O； Or R 8 , R 9 and the carbon atoms to which they are bonded together form a 3, 4, 5 or 6-membered spirocarbocycle, or a 4, 5 or 6-membered spirocyclic heterocycle, and the heteroatom is 1 or 2 N or O;
或R 10、R 11与它们所键合的碳原子一起形成3、4、5或6元螺碳环，或4、5或6元螺环杂环，所述杂原子为1或2个N或O； Or R 10 , R 11 and the carbon atoms to which they are bonded together form a 3-, 4-, 5- or 6-membered spirocarbocyclic ring, or a 4-, 5- or 6-membered spirocyclic heterocycle, and the heteroatom is 1 or 2 N or O;
或R 6、R 8形成1或2个碳桥环； Or R 6 and R 8 form 1 or 2 carbon bridge rings;
或R 6、R 10形成1或2个碳桥环； Or R 6 and R 10 form 1 or 2 carbon bridge rings;
或R 8、R 10形成1或2个碳桥环； Or R 8 and R 10 form 1 or 2 carbon bridge rings;
或R 14、R 6形成3、4、5或6个碳稠合环； Or R 14 , R 6 form 3, 4, 5 or 6 carbon fused rings;
或R 14、R 10形成3、4、5或6个碳稠环； Or R 14 and R 10 form 3, 4, 5 or 6 carbon fused rings;
或R 14、R 8形成1或2个碳桥环； Or R 14 and R 8 form 1 or 2 carbon bridge rings;
或R 14、R 4形成3、4、5或6碳稠合环，且R 4在连接R 14的碳α上或形成1、2、3或4碳桥环，且R 4不在连接R 14的碳α上； Or R 14 , R 4 form a 3, 4, 5 or 6 carbon fused ring, and R 4 is on the carbon α attached to R 14 or forms a 1, 2, 3 or 4 carbon bridged ring, and R 4 is not attached to R 14 on carbon α;
R 12为连接目标配体的链； R 12 is the chain connecting the target ligand;
R 5、R 14分别选自氢、烷基、烯烃、炔烃、卤素、羟基、烷氧基、叠氮基、氨基、氰基、-NH(脂肪族，包括烷基)、-N(脂肪族，包括烷基) 2、-NHSO 2(脂肪族，包括烷基)、-N(脂肪族，包括烷基)SO 2烷基、-NHSO 2(芳基，杂芳基或杂环)、C(O)R 4、-N(烷基)SO 2(芳基，杂芳基或杂环)、-NHSO 2烯基、-N(烷基)SO 2烯基、-NHSO 2炔基、-N(烷基)SO 2炔基、卤代烷基、脂族、杂脂族、芳基、杂芳基、杂烷基和碳环； R 5 and R 14 are respectively selected from hydrogen, alkyl, alkene, alkyne, halogen, hydroxyl, alkoxy, azide, amino, cyano, -NH (aliphatic, including alkyl), -N (aliphatic) family, including alkyl) 2 , -NHSO 2 (aliphatic, including alkyl), -N (aliphatic, including alkyl) SO 2 alkyl, -NHSO 2 (aryl, heteroaryl or heterocycle), C(O)R 4 , -N(alkyl)SO 2 (aryl, heteroaryl or heterocycle), -NHSO 2 alkenyl, -N(alkyl) SO 2 alkenyl, -NHSO 2 alkynyl, -N(alkyl) SO2alkynyl , haloalkyl, aliphatic, heteroaliphatic, aryl, heteroaryl, heteroalkyl and carbocyclic;
其中每个R 5可以任选地被一个或多个选自烷基、烯烃、炔烃、卤素、羟基、烷氧基、叠氮基、氨基、-NH烷基、-N(烷基) 2、芳基、杂环烷基、杂芳基、卤代烷基和环烷基； wherein each R5 may optionally be replaced by one or more selected from the group consisting of alkyl, alkene, alkyne, halogen, hydroxy, alkoxy, azide, amino, -NHalkyl, -N(alkyl) 2 , aryl, heterocycloalkyl, heteroaryl, haloalkyl and cycloalkyl;
R 16为
Figure PCTCN2022088560-appb-000368
Figure PCTCN2022088560-appb-000369
R 16 is
Figure PCTCN2022088560-appb-000368
Figure PCTCN2022088560-appb-000369
在一些实施方案中，所述E17、E17a、E17b和E17c中，R 1、R 4、R 10、R 11、R 14、R 16、W 1、W 2、X、
Figure PCTCN2022088560-appb-000370
和n”如WO2018/237026中所定义，其全部内容通过引用并入本文。 In some embodiments, in the E17, E17a, E17b and E17c, R 1 , R 4 , R 10 , R 11 , R 14 , R 16 , W 1 , W 2 , X,
Figure PCTCN2022088560-appb-000370
and n" are as defined in WO2018/237026, the entire contents of which are incorporated herein by reference.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E18、E18a、E18b、E18c、E18d、E18e、E18f、E18g、E18h、E18i、E18g、E18k、E18l或E18m：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of E18, E18a, E18b, E18c, E18d, E18e, E18f, E18g, E18h, E18i, E18g, E18k, E181 or E18m:
Figure PCTCN2022088560-appb-000371
Figure PCTCN2022088560-appb-000371
Figure PCTCN2022088560-appb-000372
Figure PCTCN2022088560-appb-000372
其中所述E18、E18a、E18b、E18c、E18d、E18e、E18f、E18g、E18h、E18i、E18g、E18k、E18l和E18m中：Wherein said E18, E18a, E18b, E18c, E18d, E18e, E18f, E18g, E18h, E18i, E18g, E18k, E18l and E18m:
X 1为-C(R) 2、-O-、-NR-、-CF 2-、
Figure PCTCN2022088560-appb-000373
-C(O)-、-C(S)-或者
Figure PCTCN2022088560-appb-000374
X 1 is -C(R) 2 , -O-, -NR-, -CF 2 -,
Figure PCTCN2022088560-appb-000373
-C(O)-, -C(S)- or
Figure PCTCN2022088560-appb-000374
X 2和X 3各自独立的为-CH 2-、-C(O)-、-C(S)-、-C(R) 2C(O)-或者
Figure PCTCN2022088560-appb-000375
X 2 and X 3 are each independently -CH 2 -, -C(O)-, -C(S)-, -C(R) 2 C(O)- or
Figure PCTCN2022088560-appb-000375
Z 1和Z 2各自独立的为碳原子或者氮原子； Z 1 and Z 2 are each independently a carbon atom or a nitrogen atom;
环A x选自苯基、4-6元饱和的或是部分不饱和的环烷基或是含有1-3个选自N、O或S杂原子的杂环烷基、5-6元含有1-4个选自N、O或S杂原子的杂芳基； Ring A x is selected from phenyl, 4-6 membered saturated or partially unsaturated cycloalkyl or heterocycloalkyl containing 1-3 heteroatoms selected from N, O or S, 5-6 membered containing 1-4 heteroaryl groups selected from N, O or S heteroatoms;
L x为键或者C 1-C 3亚烷基，所述亚烷基中的1-2个亚甲基任选的被选自-O-、-S-、-C(O)-、-C(S)-、-C(R) 2-、-CRF、-CF 2-、-NR-、-S(O) 2-、-CH＝CH-或者亚炔基的基团所替代； L x is a bond or a C 1 -C 3 alkylene group, and 1-2 methylene groups in the alkylene group are optionally selected from -O-, -S-, -C(O)-, - C(S)-, -C(R) 2 -, -CRF, -CF 2 -, -NR-, -S(O) 2 -, -CH=CH- or alkynylene group;
R x选自氢、氘、-R z、卤素、-CN、-NO 2、-OR、-SR、-N(R) 2、-S(O)R、-S(O) 2R、-S(O) 2N(R) 2、-CF(R) 2-、-CF 2R-、-CF 3-、-C(R) 2(OR)-、-C(R) 2[N(R) 2]-、-C(O)R、-C(O)OR、-C(O)N(R) 2、-C(O)N(R)OR、-OC(O)R、-OC(O)N(R) 2、-C(S)NR 2、-NRC(O)OR、-NRC(O)R、-NRC(O)N(R) 2、-NRS(O) 2R、-C(R) 2N(R)C(O)R、-C(R) 2N(R)C(O)N(R) 2、-OP(O)(R) 2、-OP(O)(OR) 2、-OP(O)(OR)[N(R) 2]、-OP(O)[N(R) 2]、-NP(O)(R) 2、-NRP(O)(OR) 2、-N(R)P(O)(OR)[N(R) 2]、-N(R)P(O)[N(R) 2] 2、-Si(OR)R 2或-SiR 3；或者 Rx is selected from hydrogen, deuterium, -Rz , halogen, -CN, -NO2 , -OR, -SR, -N(R) 2 , -S(O)R, -S(O ) 2R, - S(O) 2 N(R) 2 , -CF(R) 2 -, -CF 2 R-, -CF 3 -, -C(R) 2 (OR)-, -C(R) 2 [N( R) 2 ]-, -C(O)R, -C(O)OR, -C(O)N(R) 2 , -C(O)N(R)OR, -OC(O)R, - OC(O)N(R) 2 , -C(S)NR 2 , -NRC(O)OR, -NRC(O)R, -NRC(O)N(R) 2 , -NRS(O) 2 R , -C(R) 2 N(R)C(O)R, -C(R) 2 N(R)C(O)N(R) 2 , -OP(O)(R) 2 , -OP( O)(OR) 2 , -OP(O)(OR)[N(R) 2 ], -OP(O)[N(R) 2 ], -NP(O)(R) 2 , -NRP(O )(OR) 2 , -N(R)P(O)(OR)[N(R) 2 ], -N(R)P(O)[N(R) 2 ] 2 , -Si(OR)R 2 or -SiR 3 ; or
两个R x与其所连接的原子一起形成任选被取代的5-8元部分不饱和的或者芳基稠和的含有0-2个选自N、O或S杂原子的杂环烷基； Two R x together with the atoms to which they are attached form an optionally substituted 5-8 membered partially unsaturated or aryl-fused heterocycloalkyl containing 0-2 heteroatoms selected from N, O or S;
每个R各自独立的为氢、或者任选被取代的选自C 1-C 6烷基、苯基、4-7元饱和的或者部分不饱和的含有1-2个选自N、O或者S杂原子的杂环烷基、5-6元含有1-4个选自N、O或者S杂原子的杂芳基环；或者 Each R is independently hydrogen, or optionally substituted selected from C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated containing 1-2 members selected from N, O or Heterocycloalkyl with S heteroatom, 5-6 membered heteroaryl ring containing 1-4 heteroatoms selected from N, O or S; or
相同碳原子上或者相同氮原子上的两个R与其所连接的原子一起形成任选被取代的4-7元饱和的或者部分不饱和的环烷基或者杂环烷基、或者形成含有1-4个选自N、O或者S杂原子的杂芳基；Two Rs on the same carbon atom or on the same nitrogen atom together with the atoms to which they are attached form an optionally substituted 4-7 membered saturated or partially unsaturated cycloalkyl or heterocycloalkyl, or a cycloalkyl containing 1- 4 heteroaryl groups selected from N, O or S heteroatoms;
R y选自氢或者
Figure PCTCN2022088560-appb-000376
R y is selected from hydrogen or
Figure PCTCN2022088560-appb-000376
环B x选自苯基、4-10元饱和的或者部分不饱和的单环或者双环环烷基或者含有1-3个选自N、O或者S杂原子的杂环烷基、或者5-6元含有1-4个选自N、O或者S杂原子的杂芳基，所述环B x进一步任选被1-2个氧代基取代； Ring B x is selected from phenyl, 4-10 membered saturated or partially unsaturated monocyclic or bicyclic cycloalkyl or heterocycloalkyl containing 1-3 heteroatoms selected from N, O or S, or 5- 6-membered heteroaryl group containing 1-4 heteroatoms selected from N, O or S, and the ring B x is further optionally substituted by 1-2 oxo groups;
每个R w各自独立的选自氢、氘代、R z、卤素、-CN、-NO 2、-OR、-SR、-N(R) 2、-S(O)R、-S(O) 2R、-S(O) 2N(R) 2、-CF(R) 2-、-CF 2R-、-CF 3-、-C(R) 2(OR)-、-C(R) 2[N(R) 2]-、-C(O)R、-C(O)OR、-C(O)N(R) 2、-C(O)N(R)OR、-OC(O)R、-OC(O)N(R) 2、-C(S)NR 2、-NRC(O)OR、-NRC(O)R、-NRC(O)N(R) 2、-NRS(O) 2R、-C(R) 2N(R)C(O)R、-C(R) 2N(R)C(O)N(R) 2、-OP(O)(R) 2、-OP(O)(OR) 2、-OP(O)(OR)[N(R) 2]、-OP(O)[N(R) 2]、-NP(O)(R) 2、-NRP(O)(OR) 2、-N(R)P(O)(OR)[N(R) 2]、-N(R)P(O)[N(R) 2] 2、-Si(OR)R 2或-SiR 3； Each R w is independently selected from hydrogen, deuterated, R z , halogen, -CN, -NO 2 , -OR, -SR, -N(R) 2 , -S(O)R, -S(O ) 2 R, -S(O) 2 N(R) 2 , -CF(R) 2 -, -CF 2 R-, -CF 3 -, -C(R) 2 (OR)-, -C(R ) 2 [N(R) 2 ]-, -C(O)R, -C(O)OR, -C(O)N(R) 2 , -C(O)N(R)OR, -OC( O)R, -OC(O)N(R) 2 , -C(S)NR 2 , -NRC(O)OR, -NRC(O)R, -NRC(O)N(R) 2 , -NRS (O) 2 R, -C(R) 2 N(R)C(O)R, -C(R) 2 N(R)C(O)N(R) 2 , -OP(O)(R) 2 , -OP(O)(OR) 2 , -OP(O)(OR)[N(R) 2 ], -OP(O)[N(R) 2 ], -NP(O)(R) 2 , -NRP(O)(OR) 2 , -N(R)P(O)(OR)[N(R) 2 ], -N(R)P(O)[N(R) 2 ] 2 , - Si(OR)R 2 or -SiR 3 ;
每个R z各自独立的为C 1-C 6烷基、苯基、4-7元饱和的或者部分不饱和的含有1-2个选自N、O或者S杂原子的杂环烷基、5-6元含有1-4个选自N、O或者S杂原子的杂芳基环； Each R z is independently C 1 -C 6 alkyl, phenyl, 4-7 membered saturated or partially unsaturated heterocycloalkyl containing 1-2 heteroatoms selected from N, O or S, 5-6 membered heteroaryl rings containing 1-4 heteroatoms selected from N, O or S;
x为0、1、2、3或4；x is 0, 1, 2, 3, or 4;
y为0、1或2；y is 0, 1 or 2;
w为0、1、2、3或4。w is 0, 1, 2, 3, or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E19、E19a、E19b、E19c、E19d、E19e、E19f、E19g、E19h或E19i：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of E19, E19a, E19b, E19c, E19d, E19e, E19f, E19g, E19h or E19i:
Figure PCTCN2022088560-appb-000377
Figure PCTCN2022088560-appb-000377
其中所述E19、E19a、E19b、E19c、E19d、E19e、E19f、E19g、E19h和E19i中：wherein said E19, E19a, E19b, E19c, E19d, E19e, E19f, E19g, E19h and E19i:
A 1为-C(R 16a)＝或-N＝； A 1 is -C(R 16a )= or -N=;
A 2为-C(R 16b)＝或-N＝； A 2 is -C(R 16b )= or -N=;
A 3为-C(R 16c)＝或-N＝； A 3 is -C(R 16c )= or -N=;
G为-C(R 16d)＝或-N＝； G is -C(R 16d )= or -N=;
Z为-CH 2或-C(＝O)-； Z is -CH 2 or -C(=O)-;
R 5为H、甲基或F； R 5 is H, methyl or F;
R 16a、R 16b、R 16c和R 16d各自独立地选自H、卤素或C 1-C 4烷基。 R 16a , R 16b , R 16c and R 16d are each independently selected from H, halogen or C 1 -C 4 alkyl.
在一些实施方案中，所述E19、E19a、E19b、E19c、E19d、E19e、E19f、E19g、E19h和E19i中，A 1、A 2、A 3、Z、G和R 5如WO2017/176958(其全文通过引用的方式并入本文中)中所定义和描述。 In some embodiments, in said E19, E19a, E19b, E19c, E19d, E19e, E19f, E19g, E19h and E19i, A 1 , A 2 , A 3 , Z, G and R 5 are as described in WO2017/176958 (which is hereby incorporated by reference in its entirety as defined and described in .
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E20、E20a、E20b、E20c、E20d、E20e或E20f：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E20, E20a, E20b, E20c, E20d, E20e or E20f:
Figure PCTCN2022088560-appb-000378
Figure PCTCN2022088560-appb-000378
其中所述E20、E20a、E20b、E20c、E20d、E20e和E20f中：Wherein said E20, E20a, E20b, E20c, E20d, E20e and E20f:
L 1选自：键、
Figure PCTCN2022088560-appb-000379
Figure PCTCN2022088560-appb-000380
L1 is selected from : key,
Figure PCTCN2022088560-appb-000379
Figure PCTCN2022088560-appb-000380
Figure PCTCN2022088560-appb-000381
Figure PCTCN2022088560-appb-000381
或者
Figure PCTCN2022088560-appb-000382
or
Figure PCTCN2022088560-appb-000382
X 1、X 2、X 3和X 4各自独立的选自氮或者CR 4，且X 1、X 2、X 3和X 4中最多两个同时选自氮； X 1 , X 2 , X 3 and X 4 are each independently selected from nitrogen or CR 4 , and at most two of X 1 , X 2 , X 3 and X 4 are simultaneously selected from nitrogen;
Z 2和Z 3选自-CH 2-或-C(O)-且Z 1和Z 2中至少有一个选自-C(O)-； Z 2 and Z 3 are selected from -CH 2 - or -C(O)- and at least one of Z 1 and Z 2 is selected from -C(O)-;
o选自0、1、2、3或4；o is selected from 0, 1, 2, 3 or 4;
每个R 4各自独立的选自氢、卤素、羟基、C 1-C 6烷基、C 1-C 6烷氧基或C 1-C 6卤代烷基； Each R 4 is independently selected from hydrogen, halogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkyl;
每个R 5各自独立的选自氢、C 1-C 6烷基或-C(O)-烷基； Each R 5 is independently selected from hydrogen, C 1 -C 6 alkyl or -C(O)-alkyl;
每个R 8各自独立的选自氢、C 1-C 6烷基或C 1-C 6卤代烷基；或者两个R 8与其所连接的原子一起相处环丙基。 Each R 8 is independently selected from hydrogen, C 1 -C 6 alkyl or C 1 -C 6 haloalkyl; or two R 8 together with the atom to which they are attached are cyclopropyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E21:The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E21:
Figure PCTCN2022088560-appb-000383
Figure PCTCN2022088560-appb-000383
其中所述E21中：Among the E21:
X”为C或N；X" is C or N;
Y”为C、N、O或者S；Y" is C, N, O or S;
Q 1、Q 2、Q 3、Q 4、Q 5各自独立的为CR 3”或N； Q 1 , Q 2 , Q 3 , Q 4 , Q 5 are independently CR 3 ″ or N;
R 3”各自独立的为氢、氘、羟基、氨基、氰基、卤素、C 1-C 6烷基、C 3-C 8环烷基、3-8元杂环烷基(例如吗啉基，例如
Figure PCTCN2022088560-appb-000384
)、6-10元芳基、5-10元杂芳基、-O(C 1-C 6烷基)、-O-(C 3-C 8环烷基)、-O-(3-8元杂环烷基)、N(C 1-C 6烷基) 1-2、NH(C 3-C 8环烷基)、NH(3-8元杂环烷基)、-O-(6-10芳基)、-O-(5-10元杂芳基)；所述烷基、环烷基、杂环烷基、芳基、杂芳基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代； R 3 " is each independently hydrogen, deuterium, hydroxy, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl (eg morpholinyl ,E.g
Figure PCTCN2022088560-appb-000384
), 6-10-membered aryl, 5-10-membered heteroaryl, -O(C 1 -C 6 alkyl), -O-(C 3 -C 8 cycloalkyl), -O-(3-8 membered heterocycloalkyl), N(C 1 -C 6 alkyl) 1-2 , NH(C 3 -C 8 cycloalkyl), NH(3-8 membered heterocycloalkyl), -O-(6 -10 aryl), -O-(5-10 membered heteroaryl); the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally selected by 1-3 independent Substituted from hydroxyl, halogen, cyano, amino groups;
m”为1、2或3；m" is 1, 2 or 3;
R 1”各自独立的为氢、氘、羟基、氨基、氰基、卤素、C 1-C 6烷基、C 3-C 8环烷基、3-8元杂环烷基、6-10元芳基、5-10元杂芳基、-O(C 1-C 6烷基)，所述烷基、环烷基、杂环烷基、芳基、杂芳基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代； R 1 " is independently hydrogen, deuterium, hydroxyl, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, 6-10 membered Aryl, 5-10 membered heteroaryl, -O(C 1 -C 6 alkyl), the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally substituted by 1-3 substituted with groups independently selected from hydroxyl, halogen, cyano, amino;
R 2”为氢、氘、C 1-C 6烷基或者C 3-C 6环烷基，所述C 1-C 6烷基和C 3-C 6环烷基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代。 R 2 " is hydrogen, deuterium, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, and the C 1 -C 6 alkyl and C 3 -C 6 cycloalkyl are optionally surrounded by 1-3 substituted with a group independently selected from hydroxy, halogen, cyano, amino.
本发明某些实施方式中，所述E21中的Q 1、Q 2、Q 3、Q 4、Q 5中的1个或者2个为N，其余各自独立的为CR 3”。 In some embodiments of the present invention, one or two of Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 in the E21 are N, and the rest are independently CR 3 ″.
本发明某些实施方式中，所述E21中的Q 1、Q 2、Q 3、Q 4、Q 5各自独立的为CR 3”。 In some embodiments of the present invention, Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 in the E21 are each independently CR 3 ″.
本发明某些实施方式中，所述E21中的X”为N。In some embodiments of the present invention, X" in the E21 is N.
本发明某些实施方式中，所述E21中的X”为C。In some embodiments of the present invention, X" in the E21 is C.
本发明某些实施方式中，所述E21中的Y”为N。In some embodiments of the present invention, Y" in the E21 is N.
本发明某些实施方式中，所述E21中的R 1”各自独立的为氢、氘、-F、-Cl、或C 1-C 6烷基，所述烷基任选被1-3个卤素取代；优选R 1”为氢。 In certain embodiments of the present invention, each of R 1 " in the E21 is independently hydrogen, deuterium, -F, -Cl, or C 1 -C 6 alkyl, and the alkyl is optionally replaced by 1-3 Halogen substituted ; preferably R1" is hydrogen.
本发明某些实施方式中，所述E21中的R 2”为氢或C 1-C 6烷基，所述烷基任选被1-3个卤素取代；优选R 2”为氢。 In certain embodiments of the present invention, R 2 " in the E21 is hydrogen or C 1 -C 6 alkyl, and the alkyl is optionally substituted with 1-3 halogens; preferably R 2 " is hydrogen.
本发明某些实施方式中，所述E21中的R 3”各自独立的为氢、氘、卤素、-O(C 1-C 6烷基)、或C 1-C 6烷基，所述烷基任选被1-3个卤素取代；优选R 3”各自独立的为氢、氘、F、Cl、甲基、甲氧基、乙氧基、三氟甲氧基、2-羟基丙-2基或三氟甲基。 In certain embodiments of the present invention, R 3 " in the E21 is each independently hydrogen, deuterium, halogen, -O(C 1 -C 6 alkyl), or C 1 -C 6 alkyl, the alkane The group is optionally substituted by 1-3 halogens; preferably R 3 " is independently hydrogen, deuterium, F, Cl, methyl, methoxy, ethoxy, trifluoromethoxy, 2-hydroxypropan-2 group or trifluoromethyl.
本发明某些实施方式中，所述E21中的m为2。In some embodiments of the present invention, m in the E21 is 2.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000385
Figure PCTCN2022088560-appb-000385
其中所述Q 1、Q 2、Q 3、Q 4、Q 5、R 1”、R 2”、m”如上述E21中所定义。 wherein said Q 1 , Q 2 , Q 3 , Q 4 , Q 5 , R 1 ", R 2 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000386
Figure PCTCN2022088560-appb-000386
其中所述R 1”、R 2”、R 3”、m”如上述E21中所定义。 wherein said R 1 ", R 2 ", R 3 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000387
Figure PCTCN2022088560-appb-000387
其中所述R 1”、R 2”、R 3”如上述E21中所定义。本发明某些实施方式中,所述E21具有下式结构 wherein said R 1 ″, R 2 ″, R 3 ″ are as defined in E21 above. In some embodiments of the present invention, said E21 has the following structure
Figure PCTCN2022088560-appb-000388
Figure PCTCN2022088560-appb-000388
其中所述R 3”如上述E21中所定义。本发明某些实施方式中,所述E21具有下式结构 wherein said R 3 " is as defined in E21 above. In certain embodiments of the present invention, said E21 has the following structure
Figure PCTCN2022088560-appb-000389
Figure PCTCN2022088560-appb-000389
其中所述Q 1、Q 2、Q 3、Q 5、R 1”、R 2”和m”如上述E21中所定义。 wherein said Q 1 , Q 2 , Q 3 , Q 5 , R 1 ", R 2 " and m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000390
Figure PCTCN2022088560-appb-000390
其中所述R 1”、R 2”、R 3”、m”如上述E21中所定义。 wherein said R 1 ", R 2 ", R 3 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000391
Figure PCTCN2022088560-appb-000391
其中所述R 1”、R 2”、R 3”如上述E21-1中所定义。 wherein said R 1 ", R 2 ", R 3 " are as defined in E21-1 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000392
Figure PCTCN2022088560-appb-000392
其中所述R 3”如上述E21中所定义。 wherein said R 3 " is as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构：In certain embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000393
Figure PCTCN2022088560-appb-000393
其中所述R 3”如上述E21中所定义。 wherein said R 3 " is as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构：In certain embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000394
Figure PCTCN2022088560-appb-000394
Figure PCTCN2022088560-appb-000395
Figure PCTCN2022088560-appb-000395
其中所述R 3”如上述E21中所定义。 wherein said R 3 " is as defined in E21 above.
本发明某些实施方式中，所述E21和E21-1a至1j中，R 3”为氢、卤素(例如F或Cl)、C 1-C 6烷基或-O(C 1-C 6烷基)(例如-OCH 3)，所述C 1-C 6烷基和-O(C 1-C 6烷基)任选被1-3个卤素(例如F)取代。 In certain embodiments of the present invention, in the E21 and E21-1a to 1j, R 3 " is hydrogen, halogen (eg F or Cl), C 1 -C 6 alkyl or -O(C 1 -C 6 alkane group) (eg -OCH3 ), the C1 - C6 alkyl and -O( C1 - C6 alkyl) are optionally substituted with 1-3 halogens (eg F).
本发明某些实施方式中，所述E21和E21-1a至1j中，R 3”为氢、F、Cl、CF 3、-OCF 3、或-OCH 3。 In certain embodiments of the present invention, in the E21 and E21-1a to 1j, R 3 " is hydrogen, F, Cl, CF 3 , -OCF 3 , or -OCH 3 .
本发明某些优选的实施方式中，所述E21-1h，R 3”为卤素(例如F或Cl)或-O(C 1-C 6烷基)(例如-OCH 3)。 In certain preferred embodiments of the present invention, the E21-1h, R 3 " is halogen (eg F or Cl) or -O(C 1 -C 6 alkyl) (eg -OCH 3 ).
本发明某些实施方式中，所述E21-1h为下列任一结构：In certain embodiments of the present invention, the E21-1h is any of the following structures:
Figure PCTCN2022088560-appb-000396
Figure PCTCN2022088560-appb-000396
本发明某些优选的实施方式中，所述E21-1h为下列任一结构：In some preferred embodiments of the present invention, the E21-1h is any of the following structures:
Figure PCTCN2022088560-appb-000397
Figure PCTCN2022088560-appb-000397
本发明某些实施方式中，所述E21-1i为下列结构：In some embodiments of the present invention, the E21-1i has the following structure:
Figure PCTCN2022088560-appb-000398
Figure PCTCN2022088560-appb-000398
本发明某些实施方式中，所述E21-1j为下列任一结构：In some embodiments of the present invention, the E21-1j is any of the following structures:
Figure PCTCN2022088560-appb-000399
Figure PCTCN2022088560-appb-000399
本发明某些实施方式中，所述E21选自In certain embodiments of the present invention, the E21 is selected from
Figure PCTCN2022088560-appb-000400
Figure PCTCN2022088560-appb-000400
Figure PCTCN2022088560-appb-000401
Figure PCTCN2022088560-appb-000401
本发明某些实施方式中，所述E21选自In certain embodiments of the present invention, the E21 is selected from
Figure PCTCN2022088560-appb-000402
Figure PCTCN2022088560-appb-000402
本发明某些优选的实施方式中,所述E21具有下式结构：In some preferred embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000403
Figure PCTCN2022088560-appb-000403
本发明某些优选的实施方式中,所述E21具有下式结构：In some preferred embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000404
Figure PCTCN2022088560-appb-000404
本发明某些优选的实施方式中,所述E21具有下式结构：In some preferred embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000405
Figure PCTCN2022088560-appb-000405
本发明某些优选的实施方式中,所述E21具有下式结构：In some preferred embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000406
Figure PCTCN2022088560-appb-000406
本发明某些优选的实施方式中,所述E21具有下式结构：In some preferred embodiments of the present invention, the E21 has the following formula:
Figure PCTCN2022088560-appb-000407
Figure PCTCN2022088560-appb-000407
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000408
Figure PCTCN2022088560-appb-000408
其中所述Q 1、Q 2、Q 3、Q 4、Q 5、R 1”、R 2”、m”如上述E21中所定义。 wherein said Q 1 , Q 2 , Q 3 , Q 4 , Q 5 , R 1 ", R 2 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000409
Figure PCTCN2022088560-appb-000409
其中所述R 1”、R 2”、R 3”、m”如上述E21中所定义。 wherein said R 1 ", R 2 ", R 3 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000410
Figure PCTCN2022088560-appb-000410
其中所述R 1”、R 2”、R 3”如上述E21中所定义。 wherein said R 1 ", R 2 ", R 3 " are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000411
Figure PCTCN2022088560-appb-000411
其中所述R 3”如上述E21中所定义。 wherein said R 3 " is as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000412
Figure PCTCN2022088560-appb-000412
其中所述Q 1、Q 2、Q 3、Q 5、R 1”、R 2”、m”如上述E21中所定义。 wherein said Q 1 , Q 2 , Q 3 , Q 5 , R 1 ", R 2 ", m" are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000413
Figure PCTCN2022088560-appb-000413
其中所述R 1”、R 2”、R 3”、m”如上述E21-1中所定义。 wherein said R 1 ", R 2 ", R 3 ", m" are as defined in E21-1 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000414
Figure PCTCN2022088560-appb-000414
其中所述R 1”、R 2”、R 3”如上述E21中所定义。 wherein said R 1 ", R 2 ", R 3 " are as defined in E21 above.
本发明某些实施方式中,所述E21具有下式结构In some embodiments of the present invention, the E21 has the following structure
Figure PCTCN2022088560-appb-000415
Figure PCTCN2022088560-appb-000415
其中所述R 3”如上述E21中所定义。 wherein said R 3 " is as defined in E21 above.
本发明某些实施方式中，所述E21选自In certain embodiments of the present invention, the E21 is selected from
Figure PCTCN2022088560-appb-000416
Figure PCTCN2022088560-appb-000416
Figure PCTCN2022088560-appb-000417
Figure PCTCN2022088560-appb-000417
本发明某些实施方式中，所述E21选自In certain embodiments of the present invention, the E21 is selected from
Figure PCTCN2022088560-appb-000418
Figure PCTCN2022088560-appb-000418
优选地，本发明某些实施方式中，所述E21为如下任一结构：Preferably, in some embodiments of the present invention, the E21 is any one of the following structures:
Figure PCTCN2022088560-appb-000419
Figure PCTCN2022088560-appb-000419
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E22：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E22:
Figure PCTCN2022088560-appb-000420
Figure PCTCN2022088560-appb-000420
或其药学上可接受的盐，其中所述E22中：or a pharmaceutically acceptable salt thereof, wherein said E22:
R 1′为任选被取代的C 1-C 6烷基、任选被取代的-(CH 2) nOH、任选被取代的-(CH 2) nSH、任选被取代的-(CH 2) n-O-(C 1-C 6烷基)、任选被取代的-(CH 2) n-WC(O)CW-(C0-C6烷基)，其中每个W各自独立的为氢或者C1-C3烷基、任选被取代的-(CH 2) nC(O)OH、任选被取代的-(CH 2) nC(O)-(C 1-C 6烷基)、任选被取代的-(CH 2) nNHC(O)-R 1、任选被取代的-(CH 2) nC(O)-NR 1R 2、任选被取代的-(CH 2) nOC(O)-NR 1R 2、-(CH 2O) nH、任选被取代的-(CH 2) nOC(O)-(C 1-C 6烷基)、任选被取代的-(CH 2O) nC(O)OH、任选被取代的-(OCH 2) nO-(C 1-C 6烷基)、任选被取代的-(CH 2O) nC(O)-(C 1-C 6烷基)、任选被取代的-(CH 2O) nC(O)-NR 1R 2、-(CH 2CH 2O) nH、任选被取代的-(CH 2CH 2O) nCOOH、任选被取代的-(OCH 2CH 2) nO-(C 1-C 6烷基)、任选被取代的-(OCH 2CH 2) nC(O)-NR 1R 2、任选被取代的-S(O) 2R s、任选被取代的S(O)R s、硝基、氰基、或者卤素(F、Cl、Br或者I，优选F或者Cl)； R 1' is optionally substituted C 1 -C 6 alkyl, optionally substituted -(CH 2 ) n OH, optionally substituted -(CH 2 ) n SH, optionally substituted -( CH2 ) n -O-(Ci - C6alkyl ), optionally substituted-( CH2 ) n -WC(O)CW-(C0-C6alkyl), wherein each W is independently is hydrogen or C1-C3 alkyl, optionally substituted -(CH 2 ) n C(O)OH, optionally substituted -(CH 2 ) n C(O)-(C 1 -C 6 alkyl ), optionally substituted -(CH 2 ) n NHC(O)-R 1 , optionally substituted -(CH 2 ) n C(O)-NR 1 R 2 , optionally substituted -(CH 2 ) n OC(O)-NR 1 R 2 , -(CH 2 O) n H, optionally substituted -(CH 2 ) n OC(O)-(C 1 -C 6 alkyl), optionally Substituted -(CH 2 O) n C(O)OH, optionally substituted -(OCH 2 ) n O-(C 1 -C 6 alkyl), optionally substituted -(CH 2 O) n C(O)-(C 1 -C 6 alkyl), optionally substituted -(CH 2 O) n C(O)-NR 1 R 2 , -(CH 2 CH 2 O) n H, any Select substituted -(CH 2 CH 2 O) n COOH, optionally substituted -(OCH 2 CH 2 ) n O-(C 1 -C 6 alkyl), optionally substituted -(OCH 2 CH 2 ) n C(O)-NR 1 R 2 , optionally substituted -S(O) 2 R s , optionally substituted S(O)R s , nitro, cyano, or halogen (F, Cl, Br or I, preferably F or Cl);
R 1和R 2各自独立的为氢或者C 1-C 6烷基，所述烷基任选被1个或者2个羟基或者被1个、2个或者3个卤素取代(优选为F)； R 1 and R 2 are each independently hydrogen or C 1 -C 6 alkyl optionally substituted with 1 or 2 hydroxy groups or with 1, 2 or 3 halogens (preferably F);
R s为C 1-C 6烷基、任选被取代的芳基、杂芳基、或者杂环烷基或者-(CH 2) mNR 1R 2； R s is C 1 -C 6 alkyl, optionally substituted aryl, heteroaryl, or heterocycloalkyl or -(CH 2 ) m NR 1 R 2 ;
X和X’各自独立的为C(O)、C(S)、S(O)、S(O) 2(优选X和X’都为C(O))； X and X' are each independently C(O), C(S), S(O), S(O) 2 (preferably both X and X' are C(O));
R 2’为任选被取代的-(CH 2) n-C(O) u(NR 1) v(SO 2) w烷基、任选被取代的-(CH 2) n-C(O) u(NR 1) v(SO 2) wNR 1NR 2N、任选被取代的-(CH 2) n-C(O) u(NR 1) v(SO 2) w-芳基、任选被取代的-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂芳基、任选被取代的-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂环烷基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-烷基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) wNR 1NR 2N、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) wNR 1C(O)R 1N、任选被取代的-NR 1-(CH 2)n-C(O) u(NR 1) v(SO 2) w-芳基、任选被取代的-NR 1-(CH 2) n-芳基-杂芳基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂芳基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂环烷基、任选被取代的-X R2’-烷基、任选被取代的-X R2’-芳基、任选被取代的-X R2’-杂芳基、任选被取代的-X R2’-杂环烷基； R 2' is optionally substituted -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w alkyl, optionally substituted -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w NR 1N R 2N , optionally substituted -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -aryl, optionally substituted Substituted -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -heteroaryl, optionally substituted -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -heterocycloalkyl, optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -alkyl, optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w NR 1N R 2N , optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w NR 1 C(O)R 1N , optionally substituted -NR 1 -(CH 2 )nC(O) u (NR 1 ) v (SO 2 ) w -aryl radical, optionally substituted -NR 1 -(CH 2 ) n -aryl-heteroaryl, optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v ( SO 2 ) w -heteroaryl, optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -heterocycloalkyl, optionally substituted -X R2' -alkyl, optionally substituted -X R2' -aryl, optionally substituted -X R2' -heteroaryl, optionally substituted -X R2' -heterocycloalkyl;
R 3’为任选被取代的烷基、任选被取代的-(CH 2) n(O) u(NR 1)v(SO 2) w-烷基、任选被取代的-(CH 2) nC(O) u(NR 1)v(SO 2) w-NR 1NR 2N、任选被取代的-(CH 2) nC(O) u(NR 1) v(SO 2) w-C(O)NR 1R 2、任选被取代的-(CH 2) nC(O) u(NR 1) v(SO 2) w-芳基、任选被取代的-(CH 2) nC(O) u(NR 1) v(SO 2) w-杂芳基、任选被取代的-(CH 2) nC(O) u(NR 1) v(SO 2) w-杂环芳基、任选被取代的-NR 1-(CH 2)n-C(O) u(NR 1) v(SO 2) w-烷基、任选被取代的-NR 1-(CH 2)n-C(O) u(NR 1) v(SO 2) w-NR 1NR 2N、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-NR 1C(O)R 1N、 R 3' is optionally substituted alkyl, optionally substituted -(CH 2 ) n (O) u (NR 1 )v(SO 2 ) w -alkyl, optionally substituted -(CH 2 ) n C(O) u (NR 1 )v(SO 2 ) w -NR 1N R 2N , optionally substituted -(CH 2 ) n C(O) u (NR 1 ) v (SO 2 ) w - C(O)NR 1 R 2 , optionally substituted -(CH 2 ) n C(O) u (NR 1 ) v (SO 2 ) w -aryl, optionally substituted -(CH 2 ) n C(O) u (NR1) v (SO2) w - heteroaryl, optionally substituted-( CH2 ) nC (O) u (NR1) v (SO2 ) w - heteroaryl base, optionally substituted -NR 1 -(CH 2 )nC(O) u (NR 1 ) v (SO 2 ) w -alkyl, optionally substituted -NR 1 -(CH 2 )nC(O ) u (NR 1 ) v (SO 2 ) w -NR 1N R 2N , optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -NR 1 C(O)R 1N ,
任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-芳基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂芳基、任选被取代的-NR 1-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂环烷基、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-烷基、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-NR 1NR 2N、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-NR 1C(O)R 1N、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-芳基、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂芳基、任选被取代的-O-(CH 2) n-C(O) u(NR 1) v(SO 2) w-杂环烷基、-(CH 2) n-(V) n’-(CH 2) n-(V) n’-烷基、任选被取代的-(CH 2) n-(V) n’-(CH 2) n-(V) n’-芳基、任选被取代的-(CH 2) n-(V) n’-(CH 2) n-(V) n’-杂芳基、任选被取代的-(CH 2) n-(V) n’-(CH 2) n-(V) n’-杂环烷基、任选被取代的-(CH 2) n-N(R 1’)[C(O)] m’-(V) n’-烷基、任选被取代的-(CH 2) n-N(R 1’)[C(O)] m’-(V) n’-芳基、任选被取代的-(CH 2) n-N(R 1’)[C(O)] m’-(V) n’-杂芳基、任选被取代的-(CH 2) n-N(R 1’)[C(O)] m’-(V) n’-杂环烷基、任选被取代的-X R3’-烷基、任选被取代的-X R3’-芳基、任选被取代的-X R3’-杂芳基、任选被取代的-X R3’-杂环烷基、； optionally substituted -NR 1 -(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -aryl, optionally substituted -NR 1 -(CH 2 ) n -C (O) u (NR1) v (SO2) w - heteroaryl, optionally substituted -NR1-( CH2 ) n - C(O) u (NR1 ) v (SO2 ) w- Heterocycloalkyl, optionally substituted -O-(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -alkyl, optionally substituted -O-(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -NR 1N R 2N , optionally substituted -O-(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -NR 1 C(O)R 1N , optionally substituted -O-(CH 2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -aryl, optionally substituted -O-( CH2 ) n -C(O) u (NR1) v (SO2) w - heteroaryl, optionally substituted -O-( CH2 ) n -C(O) u (NR 1 ) v (SO 2 ) w -heterocycloalkyl, -(CH 2 ) n -(V) n' -(CH 2 ) n -(V) n' -alkyl, optionally substituted -(CH 2 ) n -(V) n' -(CH 2 ) n -(V) n' -aryl, optionally substituted -(CH 2 ) n -(V) n' -(CH 2 ) n -( V) n' -heteroaryl, optionally substituted-( CH2 ) n- (V) n' -( CH2 ) n- (V) n' -heterocycloalkyl, optionally substituted- ( CH2 ) n- N(R1 ' )[C(O)] m' -(V) n' -alkyl, optionally substituted-( CH2 ) n -N(R1 ' )[C (O)] m' -(V) n' -aryl, optionally substituted-( CH2 ) n -N(R1 ' )[C(O)] m' -(V) n' -hetero Aryl, optionally substituted -(CH 2 ) n -N(R 1' )[C(O)] m' -(V) n' -heterocycloalkyl, optionally substituted -X R3' -Alkyl, optionally substituted -XR3' -aryl, optionally substituted -XR3' -heteroaryl, optionally substituted -XR3' -heterocycloalkyl,;
R 1N和R 2N各自独立的为氢、任选被取代的-(CH 2) n-芳基、任选被取代的-(CH 2) n-杂芳基、任选被取代的-(CH 2) n-杂环烷基、C 1-C 6烷基，所述C 1-C 6烷基任选的被1个或2个羟基取代或者任选被1个、2个或者3 个卤素取代； R1N and R2N are each independently hydrogen, optionally substituted -( CH2 ) n -aryl, optionally substituted -( CH2 ) n -heteroaryl, optionally substituted -(CH 2 ) n -heterocycloalkyl, C1 - C6 alkyl, optionally substituted with 1 or 2 hydroxy groups or optionally with 1, 2 or 3 halogens replace;
V为O、S或者NR 1； V is O, S or NR 1 ;
R 1和R 1’各自独立的为氢或者C 1-C 3烷基； R 1 and R 1' are each independently hydrogen or C 1 -C 3 alkyl;
X R2’或者X R3’各自独立的为任选取代的-(CH 2) n-、-(CH 2) n-CH(X v)＝CH(X v)-(顺式或者反式)、-(CH 2) n-C≡CH-、-(CH 2CH 2O)-或者C 3-C 6环烷基，所述X v为氢、卤素或者任选被取代的C 1-C 3烷基； X R2' or X R3' are each independently optionally substituted -(CH 2 ) n -, -(CH 2 ) n -CH(X v )=CH(X v )-(cis or trans), -(CH 2 ) n -C≡CH-, -(CH 2 CH 2 O)- or C 3 -C 6 cycloalkyl, wherein X v is hydrogen, halogen or optionally substituted C 1 -C 3 alkyl;
m各自独立的为0、1、2、3、4、5或者6；m is independently 0, 1, 2, 3, 4, 5, or 6;
m’各自独立的为1或者；m' is independently 1 or;
n各自独立的为0、1、2、3、4、5或者6；n is independently 0, 1, 2, 3, 4, 5, or 6;
n’各自独立的为0或者1；n' is independently 0 or 1;
u各自独立的为0或者1；u are independently 0 or 1;
v各自独立的为1或者1；v is independently 1 or 1;
w各自独立的为0或者1。w is independently 0 or 1.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E23、E23a、E23b、E23c、E23d或E23e：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E23, E23a, E23b, E23c, E23d or E23e:
Figure PCTCN2022088560-appb-000421
Figure PCTCN2022088560-appb-000421
其中所述E23、E23a、E23b、E23c、E23d和E23e中：wherein said E23, E23a, E23b, E23c, E23d and E23e:
R 1'、R 2'、R 3'、X定义如E22中所述； R 1' , R 2' , R 3' , X are as defined in E22;
R 5、R 6独立地选自OH、SH或任取代的烷基；或者R 5、R 6与它们所连接的碳原子形成C＝O； R 5 , R 6 are independently selected from OH, SH or optionally substituted alkyl; or R 5 , R 6 and the carbon atoms to which they are attached form C=O;
R 7为H或任取代的烷基； R 7 is H or optionally substituted alkyl;
E为键、C＝O或C＝S；E is a bond, C=O or C=S;
G为键、任取代的烷基、-COOH或C＝J；G is a bond, optionally substituted alkyl, -COOH or C=J;
J为O或N-R 8； J is O or NR 8 ;
R 8为H、CN、任取代的烷基或任取代的烷氧基； R 8 is H, CN, optionally substituted alkyl or optionally substituted alkoxy;
M为芳基、杂芳基、杂环基或
Figure PCTCN2022088560-appb-000422
所述芳基、杂芳基、杂环基可以被任取代； M is aryl, heteroaryl, heterocyclyl or
Figure PCTCN2022088560-appb-000422
The aryl group, heteroaryl group and heterocyclic group can be optionally substituted;
R 9、R 10独自地选自H、烷基、环烷基、羟基烷基、硫代烷基、连接ULM的二硫键、杂芳基或卤代烷基，所述烷基、环烷基、羟基烷基、硫代烷基、连接ULM的二硫键、杂芳基或卤代烷基可以被任取代； 或者R 9、R 10与它们所连接的碳原子一起形成任取代的环烷基； R 9 , R 10 are independently selected from H, alkyl, cycloalkyl, hydroxyalkyl, thioalkyl, ULM-linked disulfide, heteroaryl or haloalkyl, said alkyl, cycloalkyl, Hydroxyalkyl, thioalkyl, ULM-linked disulfide, heteroaryl or haloalkyl can be optionally substituted; or R 9 , R 10 together with the carbon atoms to which they are attached form an optionally substituted cycloalkyl;
R 11为杂环烷基、烷氧基、杂芳基、芳基或
Figure PCTCN2022088560-appb-000423
所述杂环烷基、烷氧基、杂芳基、芳基可以被任取代； R 11 is heterocycloalkyl, alkoxy, heteroaryl, aryl or
Figure PCTCN2022088560-appb-000423
The heterocycloalkyl, alkoxy, heteroaryl, and aryl groups can be optionally substituted;
R 12为H或任取代的烷基； R 12 is H or optionally substituted alkyl;
R 13为H、烷基、烷基-C＝O、(环烷基)烷基-C＝O、芳烷基-C＝O、芳基-C＝O、(杂环烷基)-C＝O、芳烷基或烷氧基-C＝O，所述烷基、烷基-C＝O、(环烷基)烷基-C＝O、芳烷基-C＝O、芳基-C＝O、(杂环烷基)-C＝O、芳烷基或烷氧基-C＝O可以被任取代； R 13 is H, alkyl, alkyl-C=O, (cycloalkyl)alkyl-C=O, aralkyl-C=O, aryl-C=O, (heterocycloalkyl)-C =O, aralkyl or alkoxy-C=O, said alkyl, alkyl-C=O, (cycloalkyl)alkyl-C=O, aralkyl-C=O, aryl- C=O, (heterocycloalkyl)-C=O, aralkyl or alkoxy-C=O may be optionally substituted;
R 14为H、卤代烷基、环烷基、烷基或杂环烷基，所述环烷基、烷基或杂环烷基可以被任取代； R 14 is H, haloalkyl, cycloalkyl, alkyl or heterocycloalkyl, which may be optionally substituted;
R 15为H、杂芳基、卤代烷基、芳基、烷氧基或杂环烷基，所述杂芳基、卤代烷基、芳基、烷氧基或杂环烷基可以被任取代； R 15 is H, heteroaryl, haloalkyl, aryl, alkoxy or heterocycloalkyl, and said heteroaryl, haloalkyl, aryl, alkoxy or heterocycloalkyl may be optionally substituted;
R 16为卤素、烷基、卤代烷基、CN或卤代烷氧基，所述烷基、卤代烷基或卤代烷氧基可以被任取代； R 16 is halogen, alkyl, haloalkyl, CN or haloalkoxy, and said alkyl, haloalkyl or haloalkoxy may be optionally substituted;
R 17为H、卤素、环烷基、烷基、烯基或卤代烷基，所述环烷基、烷基、烯基可以被任取代； R 17 is H, halogen, cycloalkyl, alkyl, alkenyl or haloalkyl, and the cycloalkyl, alkyl and alkenyl may be optionally substituted;
R 23为H或OH； R 23 is H or OH;
R 25为H或取代的烷基；或者2个R 25形成＝O或取代的环烷基； R 25 is H or substituted alkyl; or 2 R 25 form =O or substituted cycloalkyl;
Z 1、Z 2、Z 3和Z 4各自独立地选自C或N； Z 1 , Z 2 , Z 3 and Z 4 are each independently selected from C or N;
X为O或S；X is O or S;
Y为H、甲基或乙基；Y is H, methyl or ethyl;
o为0、1、2、3或4。o is 0, 1, 2, 3, or 4.
在一些实施方案中，所述E23、E23a、E23b、E23c、E23d和E23e中，R 1'、R 2'、R 3'、R 5、R 6、R 7、R 9、R 10、R 11、R 14、R 15、R 16、R 17、R 23、R 25、E、M、o、X、Y、Z 1、Z 2、Z 3和Z 4如US 2016/0272639中所定义和描述，其全部内容通过引用并入本文。 In some embodiments, among the E23, E23a, E23b, E23c, E23d and E23e, R 1 ', R 2 ', R 3 ', R 5 , R 6 , R 7 , R 9 , R 10 , R 11 , R 14 , R 15 , R 16 , R 17 , R 23 , R 25 , E, M, o, X, Y, Z 1 , Z 2 , Z 3 and Z 4 are as defined and described in US 2016/0272639 , the entire contents of which are incorporated herein by reference.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E23a：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E23a:
Figure PCTCN2022088560-appb-000424
Figure PCTCN2022088560-appb-000424
其中所述E23a中：Where said E23a:
R 1’为羟基； R 1' is hydroxyl;
R 2’为-NH-CH 2-芳基-HET； R 2' is -NH-CH 2 -aryl-HET;
R 3’选自任选被取代的烷基、-(CH)R CR3’-NH-C(O)-R 3p1或者-(CH)R CR3’-R 3p2； R 3' is selected from optionally substituted alkyl, -(CH)R CR3' -NH-C(O)-R 3p1 or -(CH)R CR3' -R 3p2 ;
R CR3’为任选被取代的C 1-C 4烷基； R CR3' is optionally substituted C 1 -C 4 alkyl;
R 3p1为任选被取代的C 1-C 6烷基、任选被取代的氧杂环丁烷基、-(CH 2) nOCH 3、任选被-O(CH 2CH 3)取代的苯基或2位或者3位连接至羰基的吗啉基，所述n为1或者2； R 3p1 is optionally substituted C 1 -C 6 alkyl, optionally substituted oxetanyl, -(CH 2 ) n OCH 3 , optionally -O(CH 2 CH 3 ) substituted phenyl or morpholinyl attached to carbonyl at the 2- or 3-position, where n is 1 or 2;
R 3p2为
Figure PCTCN2022088560-appb-000425
或者任选取代的苯基； R 3p2 is
Figure PCTCN2022088560-appb-000425
or optionally substituted phenyl;
HET选自任选取代的噻唑、噁唑、异噁唑或者异噻唑；HET is selected from optionally substituted thiazoles, oxazoles, isoxazoles or isothiazoles;
R HET选自氢、卤素、氰基、任选被取代的C 1-C 6烷基、任选被取代的C 1-C 6烷氧基、任选被取代的芳基。 R HET is selected from hydrogen, halogen, cyano, optionally substituted C1 - C6 alkyl, optionally substituted C1 - C6 alkoxy, optionally substituted aryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E23cThe compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E23c
Figure PCTCN2022088560-appb-000426
Figure PCTCN2022088560-appb-000426
或其药学上可接受的盐，其中所述E23c中：or a pharmaceutically acceptable salt thereof, wherein said E23c:
每个R 5和R 6独立地是-OH、-SH或任选地被取代的烷基，或R 5、R 6和它们所连接的碳原子形成羰基； Each R5 and R6 is independently -OH, -SH or optionally substituted alkyl, or R5 , R6 and the carbon atom to which they are attached form a carbonyl group ;
R 7是H或任选地被取代的烷基； R7 is H or optionally substituted alkyl;
E是键、C＝O或C＝S；E is a bond, C=O or C=S;
G是键、任选地被取代的烷基、-COOH或C＝J；G is a bond, optionally substituted alkyl, -COOH or C=J;
J是O或N-R 8； J is O or NR 8 ;
R 8是H、CN、任选地被取代的烷基或任选地被取代的烷氧基； R is H, CN, optionally substituted alkyl or optionally substituted alkoxy;
M是任选地被取代的芳基、任选地被取代的杂芳基、任选地被取代的杂环烷基或
Figure PCTCN2022088560-appb-000427
M is optionally substituted aryl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl or
Figure PCTCN2022088560-appb-000427
每个R 9和R 10独立地是H；任选地取代的烷基、任选地被取代的环烷基、任选地被取代的羟基烷基、任选地被取代的硫基烷基、二硫键连接的ULM、任选地被取代的杂芳基或卤代烷基；或R 9、R 10和它们所连接的碳原子形成任选地被取代的环烷基； Each R9 and R10 is independently H ; optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted hydroxyalkyl, optionally substituted thioalkyl , a disulfide-linked ULM, an optionally substituted heteroaryl or haloalkyl; or R 9 , R 10 and the carbon atom to which they are attached form an optionally substituted cycloalkyl;
R 11是任选地被取代的杂环烷基、任选地被取代的烷氧基、任选地被取代的杂芳基、任选地被取代的芳基或
Figure PCTCN2022088560-appb-000428
R 11 is optionally substituted heterocycloalkyl, optionally substituted alkoxy, optionally substituted heteroaryl, optionally substituted aryl or
Figure PCTCN2022088560-appb-000428
R 12是H或任选地被取代的烷基； R12 is H or optionally substituted alkyl;
R 13是H、任选地被取代的烷基、任选地被取代的烷基羰基、任选地被取代的(环烷基)烷基羰基、任选地被取代的芳烷基羰基、任选地被取代的芳基羰基、任选地被取代的(杂环烷基)羰基或任选地被取代的芳烷基；任选地被取代的(氧代烷基)氨基甲酸酯， R 13 is H, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted (cycloalkyl)alkylcarbonyl, optionally substituted aralkylcarbonyl, optionally substituted arylcarbonyl, optionally substituted (heterocycloalkyl)carbonyl, or optionally substituted aralkyl; optionally substituted (oxoalkyl)carbamate ,
每个R 14独立地是H、卤代烷基、任选地被取代的环烷基、任选地被取代的烷基或任选地被取代的杂环烷基； each R is independently H, haloalkyl , optionally substituted cycloalkyl, optionally substituted alkyl, or optionally substituted heterocycloalkyl;
R 15是H、任选地被取代的杂芳基、卤代烷基、任选地被取代的芳基、任选地被取代的烷氧基或任选地被取代的杂环烷基； R is H, optionally substituted heteroaryl, haloalkyl, optionally substituted aryl, optionally substituted alkoxy, or optionally substituted heterocycloalkyl;
每个R 16独立地是卤素、任选地被取代的烷基、任选地被取代的卤代烷基、CN或任选地被取代的卤代烷氧基； each R is independently halogen, optionally substituted alkyl, optionally substituted haloalkyl, CN, or optionally substituted haloalkoxy;
每个R 25独立地是H或任选地被取代的烷基；或两个R 25基团可以一起形成氧代或任选地被取代的环烷基； Each R25 is independently H or optionally substituted alkyl; or two R25 groups can be taken together to form oxo or optionally substituted cycloalkyl;
R 23是H或OH； R 23 is H or OH;
Z 1、Z 2、Z 3和Z 4独立地是C或N；且 Z 1 , Z 2 , Z 3 and Z 4 are independently C or N; and
o是0、1、2、3或4。o is 0, 1, 2, 3, or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、 前药和/或其药学上可接受的盐的一个优选实施方案中，E为E23d：Compounds of formula I of the present invention, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable salts thereof In a preferred embodiment of, E is E23d:
Figure PCTCN2022088560-appb-000429
Figure PCTCN2022088560-appb-000429
其中所述E23d中：Among the E23d:
X是O或S；X is O or S;
Y是H、甲基或乙基；Y is H, methyl or ethyl;
R 17是H、甲基、乙基、羟甲基或环丙基； R 17 is H, methyl, ethyl, hydroxymethyl or cyclopropyl;
M是任选地被取代的杂芳基、任选地被取代的芳基。M is optionally substituted heteroaryl, optionally substituted aryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E23d-1The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E23d-1
Figure PCTCN2022088560-appb-000430
Figure PCTCN2022088560-appb-000430
其中所述E23d-1中：Where described in E23d-1:
Y是H、甲基或乙基；Y is H, methyl or ethyl;
R 9是H； R 9 is H;
R 10是异丙基、叔丁基、仲丁基、环戊基或环己基； R 10 is isopropyl, tert-butyl, sec-butyl, cyclopentyl or cyclohexyl;
R 11是任选地被取代的酰胺、任选地被取代的异二氢吲哚酮、任选地被取代的异噁唑、任选地被取代的杂环； R 11 is optionally substituted amide, optionally substituted isoindolinone, optionally substituted isoxazole, optionally substituted heterocycle;
R 17是H、甲基、乙基、羟甲基或环丙基。 R 17 is H, methyl, ethyl, hydroxymethyl or cyclopropyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为CN108601764(其全文通过引用的方式并入本文中)中实施例1至实施例208的具体化合物。The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is a specific compound of Example 1 to Example 208 of CN108601764, which is incorporated herein by reference in its entirety.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E24：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E24:
Figure PCTCN2022088560-appb-000431
Figure PCTCN2022088560-appb-000431
或其药学上可接受的盐，其中所述E24中：or a pharmaceutically acceptable salt thereof, wherein said E24:
X 1、X 2各自独立的选自键、O、NR Y3、CR Y3R Y4、C＝O、C＝S、SO或者SO 2； X 1 and X 2 are each independently selected from bond, O, NR Y3 , CR Y3 R Y4 , C=O, C=S, SO or SO 2 ;
R Y3、R Y4各自独立的为氢、任选被1个或多个卤素取代的C 1-C 6烷基、任选被0-3个R p取代的C 1-C 6烷氧基； R Y3 and R Y4 are each independently hydrogen, C 1 -C 6 alkyl optionally substituted by one or more halogens, C 1 -C 6 alkoxy optionally substituted by 0-3 R p ;
R p为0个、1个、2个或者3个选自氢、卤素、羟基、C 1-C 3烷基或者C(＝O)； R p is 0, 1, 2 or 3 selected from hydrogen, halogen, hydroxy, C 1 -C 3 alkyl or C(=O);
W 3选自任选被取代的T、任选被取代的-T-N(R 1aR 1b)X 3、任选被取代的-T-N(R 1aR 1b)、任选被取代的-T-芳基、任选被取代的-T-杂芳基、任选被取代的-T-双环杂芳基、任选被取代的-T-杂环烷基、任选被取代的-T-双环杂环烷基、任选被取代的-NR 1-T-芳基、任选被取代的-NR 1-T-杂芳基或者任选被取代的-NR 1-T-杂环烷基； W 3 is selected from optionally substituted T, optionally substituted -TN(R 1a R 1b )X 3 , optionally substituted -TN(R 1a R 1b ), optionally substituted -T-aryl base, optionally substituted-T-heteroaryl, optionally substituted-T-bicyclic heteroaryl, optionally substituted-T-heterocycloalkyl, optionally substituted-T-bicyclic heteroaryl cycloalkyl, optionally substituted -NR1 - T-aryl, optionally substituted -NR1 - T-heteroaryl, or optionally substituted -NR1 - T-heterocycloalkyl;
X 3为C(O)、R 1、R 1a或者R 1b； X 3 is C(O), R 1 , R 1a or R 1b ;
每个R 1、R 1a或者R 1b各自独立的选自氢、任选被1个或多个卤素或羟基取代的C1-C6烷基、R Y3C(O)、R Y3C(S)、R Y3S(O)、R Y3S(O) 2、N(R Y3R Y4)C(O)、N(R Y3R Y4)C(S)、N(R Y3R Y4)S(O)或N(R Y3R Y4)S(O) 2； Each R 1 , R 1a or R 1b is independently selected from hydrogen, C1-C6 alkyl optionally substituted with one or more halogen or hydroxy, R Y3 C(O), R Y3 C(S), R Y3 S(O), R Y3 S(O) 2 , N(R Y3 R Y4) C(O), N(R Y3 R Y4) C(S), N(R Y3 R Y4) S(O) or N(R Y3 R Y4) S(O) 2 ;
T选自任选被取代的烷基、-(CH 2) n-，所述每个亚甲基任选的被选自卤素、羟基、任选被取代的氨基酸侧链、甲基、任选被取代的烷氧基、任选被一个或者多个卤素取代的C 1-C 6烷基、-C(O)NR 1R 1a或者NR 1R 1a的取代基取代； T is selected from optionally substituted alkyl, -( CH2 ) n- , and each methylene group is optionally selected from halogen, hydroxy, optionally substituted amino acid side chain, methyl, optionally Substituted alkoxy, C 1 -C 6 alkyl optionally substituted with one or more halogens, -C(O)NR 1 R 1a or substituents of NR 1 R 1a ;
或者R 1和R 1a可任选的形成任选被取代的杂环烷基； Alternatively R 1 and R 1a may optionally form an optionally substituted heterocycloalkyl;
n为0、1、2、3、4、5或者6；n is 0, 1, 2, 3, 4, 5 or 6;
W 4为
Figure PCTCN2022088560-appb-000432
W 4 is
Figure PCTCN2022088560-appb-000432
R 14a和R 14b各自独立的为氢、卤代烷基或者任选被取代的烷基； R 14a and R 14b are each independently hydrogen, haloalkyl or optionally substituted alkyl;
W 5为任选被取代的苯基或者任选被取代的杂芳基； W 5 is optionally substituted phenyl or optionally substituted heteroaryl;
R 15为任选被取代的氢、氰基、卤素、羟基、硝基、NR 14aR 14b、OR 14a、CONR 14aR 14b、NR 14aCONR 14b、SO 2NR 14aR 14b、NR 14aSO 2R 14b、任选被取代的烷基、任选被取代的卤代烷基、任选被取代的卤代烷氧基、任选被取代的芳基、任选被取代的杂芳基、任选被取代的环烷基、任选被取代的杂环烷基。 R 15 is optionally substituted hydrogen, cyano, halogen, hydroxy, nitro, NR 14a R 14b , OR 14a , CONR 14a R 14b , NR 14a CONR 14b , SO 2 NR 14a R 14b , NR 14a SO 2 R 14b , optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted haloalkoxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted ring Alkyl, optionally substituted heterocycloalkyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E25或E25a:The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment, E is E25 or E25a:
Figure PCTCN2022088560-appb-000433
Figure PCTCN2022088560-appb-000433
其中所述E25和E25中：Among the E25 and E25 described:
所述W 3为任选被取代的芳基、任选被取代的杂芳基或者
Figure PCTCN2022088560-appb-000434
The W 3 is optionally substituted aryl, optionally substituted heteroaryl or
Figure PCTCN2022088560-appb-000434
R 9和R 10各自独立的为氢、任选被取代的烷基、任选被取代的环烷基、任选被取代的羟基烷基、任选被取代的杂芳基、卤代烷基，或者R 9和R 10与其所连接的碳原子一起形成任选被取代的环烷基； R 9 and R 10 are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted hydroxyalkyl, optionally substituted heteroaryl, haloalkyl, or R 9 and R 10 together with the carbon atom to which they are attached form an optionally substituted cycloalkyl;
R 11选自任选取代的杂环烷基、任选取代的烷氧基、任选取代的杂芳基、任选取代的芳基、
Figure PCTCN2022088560-appb-000435
Figure PCTCN2022088560-appb-000436
或者
Figure PCTCN2022088560-appb-000437
R 11 is selected from optionally substituted heterocycloalkyl, optionally substituted alkoxy, optionally substituted heteroaryl, optionally substituted aryl,
Figure PCTCN2022088560-appb-000435
Figure PCTCN2022088560-appb-000436
or
Figure PCTCN2022088560-appb-000437
R 12各自独立的为氢或者任选被取代的烷基； R 12 is each independently hydrogen or optionally substituted alkyl;
R 13各自独立的为氢、任选取代的烷基、任选取代的烷基羰基、任选取代的(环烷基)烷基羰基、任选取代的芳烷基羰基、任选取代芳基羰基、任选取代的(杂环烷基)羰基或者任选取代的芳烷基； R 13 is each independently hydrogen, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted (cycloalkyl)alkylcarbonyl, optionally substituted aralkylcarbonyl, optionally substituted aryl carbonyl, optionally substituted (heterocycloalkyl)carbonyl, or optionally substituted aralkyl;
R 14a、R 14b各自独立的为氢、卤代烷基或者任选取代的烷基； R 14a and R 14b are each independently hydrogen, haloalkyl or optionally substituted alkyl;
W 5选自任选取代的苯基或者任选取代的5-10元杂芳基； W is selected from optionally substituted phenyl or optionally substituted 5-10 -membered heteroaryl;
R 15为任选被取代的氢、氰基、卤素、羟基、硝基、NR 14aR 14b、OR 14a、CONR 14aR 14b、NR 14aCONR 14b、SO 2NR 14aR 14b、NR 14aSO 2R 14b、任选被取代的烷基、任选被取代的卤代烷基、任选被取代的卤代烷氧基、任选被取代的芳基、任选被取代的杂芳基、任选被取代的环烷基、任选被取代的杂环烷基； R 15 is optionally substituted hydrogen, cyano, halogen, hydroxy, nitro, NR 14a R 14b , OR 14a , CONR 14a R 14b , NR 14a CONR 14b , SO 2 NR 14a R 14b , NR 14a SO 2 R 14b , optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted haloalkoxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted ring alkyl, optionally substituted heterocycloalkyl;
每个R 16各自独立的为卤素、氰基、任选被取代的烷基、任选被取代的卤代烷基、任选被取代的烷氧基、羟基或者任选被取代的卤代烷基； Each R is independently halogen , cyano, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted alkoxy, hydroxy, or optionally substituted haloalkyl;
o为0、1、2、3或者4；o is 0, 1, 2, 3 or 4;
R 18各自独立的选自卤素、任选取代的烷氧基、氰基、任选取代的烷基、卤代烷基、卤代烷氧基； R 18 is each independently selected from halogen, optionally substituted alkoxy, cyano, optionally substituted alkyl, haloalkyl, haloalkoxy;
p为0、1、2、3或者4。p is 0, 1, 2, 3 or 4.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为26、E26a或E26b,The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is 26, E26a or E26b,
Figure PCTCN2022088560-appb-000438
Figure PCTCN2022088560-appb-000438
或其药学上可接受的盐，其中所述E26、E26a和E26b中,or a pharmaceutically acceptable salt thereof, wherein said E26, E26a and E26b,
R 1是氢、甲基、乙基、异丙基、叔丁基、仲丁基、环丙基、环丁基、环戊基、环己基，任选取代的烷基、任选取代的羟基烷基、任选取代的杂芳基或卤代烷基； R 1 is hydrogen, methyl, ethyl, isopropyl, tert-butyl, sec-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, optionally substituted alkyl, optionally substituted hydroxy alkyl, optionally substituted heteroaryl or haloalkyl;
R 14a是氢、卤代烷基、任选取代的烷基、甲基、氟代甲基、羟基甲基、乙基、异丙基、或环丙基； R 14a is hydrogen, haloalkyl, optionally substituted alkyl, methyl, fluoromethyl, hydroxymethyl, ethyl, isopropyl, or cyclopropyl;
X为CH 2或者C(O)； X is CH 2 or C(O);
R 15选自氢、卤素、CN、羟基、硝基、任选取代的杂芳基、任选取代的芳基、任选取代的烷基、任选取代的卤代烷基、任选取代的卤代烷氧基、任选取代的环烷基或任选取代的杂环烷基； R 15 is selected from hydrogen, halogen, CN, hydroxyl, nitro, optionally substituted heteroaryl, optionally substituted aryl, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted haloalkoxy group, optionally substituted cycloalkyl, or optionally substituted heterocycloalkyl;
R 3不存在或者为任选被取代的5-6元杂芳基。 R3 is absent or is an optionally substituted 5-6 membered heteroaryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E27、E27a、E27b、E27c、E27d、E27e、E27f和E27g：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E27, E27a, E27b, E27c, E27d, E27e, E27f and E27g:
Figure PCTCN2022088560-appb-000439
Figure PCTCN2022088560-appb-000439
其中所述E27、E27a、E27b、E27c、E27d、E27e、E27f和E27g中，X选自碳、氧、硫、亚砜、砜和N-R a； wherein in the E27, E27a, E27b, E27c, E27d, E27e, E27f and E27g , X is selected from carbon, oxygen, sulfur, sulfoxide, sulfone and NRa;
R a独立地是H或碳数目为1至6的烷基； R is independently H or an alkyl group having a carbon number of 1 to 6;
Y和Z独立地是碳或氮；Y and Z are independently carbon or nitrogen;
A、A'和A”独立地选自C、N、O或S，也可以是形成稠合双环环、或6,5和5,5-稠合的芳族双环基团的一个或两个原子；A, A' and A" are independently selected from C, N, O or S, and may also be one or both of the groups forming a fused bicyclic ring, or a 6,5 and 5,5-fused aromatic bicyclic group atom;
R 1、R 2独立地选自芳基或杂芳基、具有独立地选自硫或氮的一个或两个杂原子的杂芳基，其中所述芳基或杂芳基可以是单环或双环、或未取代的或被一至三个取代基取代，所述取代基独立地选自：卤素、-CN、C1至C6烷基、C3至C6环烷基、-OH、具有1至6个碳的烷氧基、具有1至6个碳的氟取代的烷氧基、具有1至6个碳的亚砜、具有1至6个碳的砜、具有2至6个碳的酮、具有2至6个碳的酰胺和具有2至6个碳的二烷基胺； R 1 , R 2 are independently selected from aryl or heteroaryl, heteroaryl with one or two heteroatoms independently selected from sulfur or nitrogen, wherein the aryl or heteroaryl may be monocyclic or Bicyclic, or unsubstituted or substituted with one to three substituents independently selected from: halogen, -CN, C1 to C6 alkyl, C3 to C6 cycloalkyl, -OH, having 1 to 6 Carbon alkoxy, fluorine substituted alkoxy with 1 to 6 carbons, sulfoxides with 1 to 6 carbons, sulfones with 1 to 6 carbons, ketones with 2 to 6 carbons, 2 Amides of to 6 carbons and dialkylamines of 2 to 6 carbons;
R 3、R 4独立地选自H、甲基和C 1至C 6烷基； R 3 , R 4 are independently selected from H, methyl and C 1 to C 6 alkyl;
R 5选自芳基或杂芳基、具有独立地选自硫或氮的一个或两个杂原子的杂芳基，其中所述芳基或杂芳基可以是单环或双环、或未取代的或被一至三个取代基取代，所述取代基独立地选自：卤素、-CN、C 1至C 6烷基、C 3至C 6环烷基、-OH、具有1至6个碳的烷氧基、具有1至6个碳的氟取代的烷氧基、具有1至6个碳的亚砜、具有1至6个碳的砜、具有2至6个碳的酮、具有2至6个碳的酰胺、具有2至6个碳的二 烷基胺、烷基醚(C 2至C 6)、烷基酮(C 3至C 6)、吗啉基、烷基酯(C 3至C 6)、烷基氰(C 3至C 6)； R is selected from aryl or heteroaryl, heteroaryl with one or two heteroatoms independently selected from sulfur or nitrogen, wherein the aryl or heteroaryl may be monocyclic or bicyclic, or unsubstituted or substituted by one to three substituents independently selected from: halogen, -CN, C1 to C6 alkyl, C3 to C6 cycloalkyl, -OH, having 1 to 6 carbons alkoxy, fluorine-substituted alkoxy having 1 to 6 carbons, sulfoxides having 1 to 6 carbons, sulfones having 1 to 6 carbons, ketones having 2 to 6 carbons, ketones having 2 to 6 carbons Amides of 6 carbons, dialkylamines with 2 to 6 carbons, alkyl ethers (C2 to C6 ), alkyl ketones (C3 to C6 ) , morpholinyl, alkyl esters (C3 to C 6 ), alkyl cyanide (C 3 to C 6 );
R 6为H或-C(＝O)R b，其中 R 6 is H or -C(=O)R b , wherein
R b选自烷基，环烷基，单取代、二取代或三取代的芳基或杂芳基，4-吗啉基，1-(3-氧代哌嗪基)，1-哌啶基，4-N-R c-吗啉基，4-R c-1-哌啶基和3-R c-1-哌啶基，其中 R b is selected from alkyl, cycloalkyl, mono-, di- or tri-substituted aryl or heteroaryl, 4-morpholinyl, 1-(3-oxopiperazinyl), 1-piperidinyl , 4-NR c -morpholinyl, 4-R c -1-piperidinyl and 3-R c -1-piperidinyl, wherein
R c选自烷基，氟取代的烷基，氰基烷基，羟基取代的烷基，环烷基，烷氧基烷基，酰胺烷基，烷基砜，烷基亚砜，烷基酰胺，芳基，杂芳基，单取代、二取代或三取代的芳基或杂芳基，CH 2CH 2R d和CH2CH2CH2R d，其中 R c is selected from the group consisting of alkyl, fluoro-substituted alkyl, cyanoalkyl, hydroxy-substituted alkyl, cycloalkyl, alkoxyalkyl, amidoalkyl, alkylsulfone, alkylsulfoxide, alkylamide , aryl, heteroaryl, mono-, di- or tri-substituted aryl or heteroaryl, CH 2 CH 2 R d and CH2CH2CH2R d , where
R d选自烷氧基、烷基砜、烷基亚砜、N-取代的甲酰胺、-NHC(O)-烷基、-NH-SO 2-烷基、芳基、取代的芳基、杂芳基、取代的杂芳基； R d is selected from alkoxy, alkyl sulfone, alkyl sulfoxide, N-substituted carboxamide, -NHC(O)-alkyl, -NH-SO2 - alkyl, aryl, substituted aryl, Heteroaryl, substituted heteroaryl;
R 7选自H、C 1至C 6烷基、环烷基、氟取代的烷基、氰基取代的烷基、5或6元杂芳基或芳基、取代的5或6元杂芳基或芳基； R 7 is selected from H, C 1 to C 6 alkyl, cycloalkyl, fluoro-substituted alkyl, cyano-substituted alkyl, 5- or 6-membered heteroaryl or aryl, substituted 5- or 6-membered heteroaryl radical or aryl;
R 8选自–R e-C(O)-R f、-R e-烷氧基、-R e-芳基、-R e-杂芳基和-R e-C(O)-R f-C(O)-R g，其中： R 8 is selected from -R e -C(O)-R f , -R e -alkoxy, -R e -aryl, -R e -heteroaryl and -R e -C(O)-R f -C(O)-R g , where:
R e为具有1至6个碳的亚烷基或键； R e is an alkylene group or bond having 1 to 6 carbons;
R f为取代的4至7元杂环； R f is a substituted 4- to 7-membered heterocycle;
R g选自芳基、杂芳基、取代的芳基或杂芳基、和4至7元杂环； R g is selected from aryl, heteroaryl, substituted aryl or heteroaryl, and 4 to 7 membered heterocycle;
R 9选自稠合双环芳族环上的单取代、二取代或三取代基，其中所述取代基独立地选自卤素、烯烃、炔烃、烷基、未取代的或被Cl或F取代的； R is selected from mono-, di-, or tri-substituents on a fused bicyclic aromatic ring, wherein the substituents are independently selected from halogen, alkene, alkyne, alkyl, unsubstituted or substituted by Cl or F of;
R 10选自芳基或杂芳基，其中所述杂芳基可以含有一个或两个杂原子如硫或氮，芳基或杂芳基可以是单环或双环的，所述芳基或杂芳基可以是未取代的或被一至三个取代基取代，包括卤素、F、Cl、-CN、烯烃、炔烃、C 1-C 6烷基、C 1-C 6环烷基、-OH、具有1至6个碳的烷氧基、具有1至6个碳的氟取代的烷氧基、具有1至6个碳的亚砜、具有1至6个碳的砜、具有2至6个碳的酮； R 10 is selected from aryl or heteroaryl, wherein the heteroaryl may contain one or two heteroatoms such as sulfur or nitrogen, the aryl or heteroaryl may be monocyclic or bicyclic, and the aryl or heteroaryl Aryl may be unsubstituted or substituted with one to three substituents, including halogen, F, Cl, -CN, alkene, alkyne, C1 - C6 alkyl, C1 - C6 cycloalkyl, -OH , alkoxy groups having 1 to 6 carbons, fluorine substituted alkoxy groups having 1 to 6 carbons, sulfoxides having 1 to 6 carbons, sulfones having 1 to 6 carbons, sulfones having 1 to 6 carbons carbon ketone;
R 11为-C(O)-N(R h)(R i)，其中R h和R i选自下述：H，C 1至C 6烷基，烷氧基取代的烷基，砜取代的烷基，芳基，杂芳基，单取代、二取代或三取代的芳基或杂芳基，烷基羧酸，杂芳基羧酸，烷基羧酸，氟取代的烷基羧酸酸，芳基取代的环烷基，杂芳基取代的环烷基；其中，R h和R i独立地选自H，连接以形成环，4-羟基环己烷；单羟基和二羟基取代的烷基(C 3至C 6)；3-羟基环丁烷；苯基-4-羧酸和取代的苯基-4-羧酸； R 11 is -C(O)-N(R h )(R i ), wherein R h and R i are selected from the following: H, C 1 to C 6 alkyl, alkoxy substituted alkyl, sulfone substituted Alkyl, aryl, heteroaryl, monosubstituted, disubstituted or trisubstituted aryl or heteroaryl, alkyl carboxylic acid, heteroaryl carboxylic acid, alkyl carboxylic acid, fluorine substituted alkyl carboxylic acid acid, aryl substituted cycloalkyl, heteroaryl substituted cycloalkyl; wherein R and R are independently selected from H , linked to form a ring, 4-hydroxycyclohexane; mono- and dihydroxy substituted alkyl (C 3 to C 6 ); 3-hydroxycyclobutane; phenyl-4-carboxylic acid and substituted phenyl-4-carboxylic acid;
R 12和R 13独立地选自H、低级烷基(C 1至C 6)、低级烯基(C 2至C 6)、低级炔基(C 2至C 6)、环烷基(4、5和6元环)、取代的环烷基、环烯基、取代的环烯基、5和6元芳基和杂芳基，R 12和R 13可以连接以形成在环上具有或不具有取代的5和6元环； R 12 and R 13 are independently selected from H, lower alkyl (C 1 to C 6 ), lower alkenyl (C 2 to C 6 ), lower alkynyl (C 2 to C 6 ), cycloalkyl (4, 5 and 6 membered rings), substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, 5 and 6 membered aryl and heteroaryl, R 12 and R 13 may be linked to form with or without on the ring Substituted 5- and 6-membered rings;
R 14选自烷基、取代的烷基、烯基、取代的烯基、芳基、取代的芳基、杂芳基、取代的杂芳基、杂环、取代的杂环、环烷基、取代的环烷基、环烯基和取代的环烯基； R 14 is selected from alkyl, substituted alkyl, alkenyl, substituted alkenyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocycle, substituted heterocycle, cycloalkyl, Substituted cycloalkyl, cycloalkenyl and substituted cycloalkenyl;
R 15为CN； R 15 is CN;
R 16选自其中一个或多个氢替换为氟的C 1-C 6烷基、C 1-C 6环烷基、C 2-C 6烯基、C 1-C 6烷基或C 3-C 6环烷基，其中一个CH 2替换为S(＝O)、-S或-S(＝O) 2的烷基或环烷基，其中末端CH 3替换为S(＝O) 2N(烷基)(烷基)、-C(＝O)N(烷基)(烷基)、-N(烷基)S(＝O) 2(烷基)、-C(＝O)2(烷基)、-O(烷基)的烷基或环烷基，其中氢替换为羟基的C1-6烷基或烷基-环烷基，3至7元环烷基或杂环烷基，任选含有-(C＝O)-基团，或5至6元芳基或杂芳基，所述杂环烷基或杂芳基可以含有独立地选自O、N或S的一至三个杂原子，并且所述环烷基、杂环烷基、芳基或杂芳基可以是未取代的或被独立地选自卤素、C 1-C 6烷基、羟基化的C 1-C 6烷基、含有硫醚的C 1-C 6烷基、醚、砜、亚砜、氟取代的醚或氰基的一至三个取代基取代； R 16 is selected from C 1 -C 6 alkyl, C 1 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkyl or C 3 - wherein one or more hydrogens are replaced by fluorine C 6 cycloalkyl in which one CH 2 is replaced by S(=O), -S or -S(=O) 2 alkyl or cycloalkyl in which terminal CH 3 is replaced by S(=O) 2 N( Alkyl)(alkyl), -C(=O)N(alkyl)(alkyl), -N(alkyl)S(=O) 2 (alkyl), -C(=O)2(alkyl) C1-6 alkyl or alkyl-cycloalkyl, 3- to 7-membered cycloalkyl or heterocycloalkyl, wherein hydrogen is replaced by hydroxy Optionally contain a -(C=O)- group, or a 5- to 6-membered aryl or heteroaryl group, which may contain one to three heterocyclic groups independently selected from O, N or S. atom, and the cycloalkyl, heterocycloalkyl, aryl, or heteroaryl group may be unsubstituted or independently selected from halogen, C1 - C6 alkyl, hydroxylated C1 - C6 alkane substituted with one to three substituents of thioether-containing C 1 -C 6 alkyl group, ether, sulfone, sulfoxide, fluorine-substituted ether or cyano group;
R 17选自(CH 2) nC(O)NR kR l，其中R k和R l独立地选自H、C 1-C 6烷基、羟基化的C 1-C 6烷基、C 1-C 6烷氧基烷基、其中一个或多个氢替换为氟的C 1-C 6烷基、其中一个碳替换为S(O)、S(O)(O)的C 1-C 6烷基、其中一个或多个氢替换为氟的C 1-C 6烷氧基烷基、其中一个或多个氢替换为氰基的C 1-C 6烷基、5和6元芳基或杂芳基、其中烷基含有1-6个碳的烷基芳基、以及其中烷基含有1-6个碳的烷基杂芳基，其中所述芳基或杂芳基可以是进一步被取代的；且n为0-6的整数； R 17 is selected from (CH 2 ) n C(O)NR k R l , wherein R k and R l are independently selected from H, C 1 -C 6 alkyl, hydroxylated C 1 -C 6 alkyl, C 1 - C6 alkoxyalkyl, C1 - C6 alkyl in which one or more hydrogens are replaced by fluorine, C1 -C in which one carbon is replaced by S(O), S(O)(O) 6 alkyl, C 1 -C 6 alkoxyalkyl in which one or more hydrogens are replaced by fluorine, C 1 -C 6 alkyl in which one or more hydrogens are replaced by cyano, 5 and 6 membered aryl or heteroaryl, alkylaryl in which the alkyl group contains 1-6 carbons, and alkylheteroaryl in which the alkyl group contains 1-6 carbons, wherein the aryl or heteroaryl group may be further substituted; and n is an integer from 0 to 6;
R 18选自取代的芳基、杂芳基、烷基、环烷基，所述取代优选为-N(C 1-C 4烷基)(环烷基)、-N(C 1-C 4烷基)烷基-环烷基、和-N(C 1-C 4烷基)[(烷基)-(杂环取代的)-环烷基； R 18 is selected from substituted aryl, heteroaryl, alkyl, cycloalkyl, and the substitution is preferably -N(C 1 -C 4 alkyl) (cycloalkyl), -N(C 1 -C 4 Alkyl)alkyl-cycloalkyl, and -N( C1 - C4alkyl)[(alkyl)-(heterocycle-substituted)-cycloalkyl;
R 19选自芳基、杂芳基、双环杂芳基，并且这些芳基或杂芳基可以被卤素、C1-6烷基、C1-6环烷基、 CF 3、F、CN、炔烃、烷基砜取代，所述卤素取代可以是单取代或三取代的； R 19 is selected from aryl, heteroaryl, bicyclic heteroaryl, and these aryl or heteroaryl may be replaced by halogen, C1-6 alkyl, C1-6 cycloalkyl, CF 3 , F, CN, alkyne , alkyl sulfone substitution, the halogen substitution can be mono-substituted or tri-substituted;
R 20和R 21独立地选自C 1-C 6烷基、C 1-C 6环烷基、C 1-C 6烷氧基、羟基化的C 1-C 6烷氧基和氟取代的C 1-C 6烷氧基，其中R 20和R 21还可以连接以形成5、6和7元环或杂环环，其可以进一步被取代； R 20 and R 21 are independently selected from C 1 -C 6 alkyl, C 1 -C 6 cycloalkyl, C 1 -C 6 alkoxy, hydroxylated C 1 -C 6 alkoxy and fluorine substituted C 1 -C 6 alkoxy, wherein R 20 and R 21 may also be linked to form 5-, 6- and 7-membered rings or heterocyclic rings, which may be further substituted;
R 22选自H、C 1-C 6烷基、C 1-C 6环烷基、羧酸、羧酸酯、酰胺、反向酰胺、磺酰胺、反向磺酰胺、N-酰基脲、含氮的5元杂环，所述5元杂环可以进一步被C 1-C 6烷基、烷氧基、氟取代的烷基、CN和烷基砜取代； R 22 is selected from H, C 1 -C 6 alkyl, C 1 -C 6 cycloalkyl, carboxylic acid, carboxylate, amide, reverse amide, sulfonamide, reverse sulfonamide, N-acylurea, containing A 5-membered heterocycle of nitrogen, which may be further substituted by C1 - C6 alkyl, alkoxy, fluorine-substituted alkyl, CN, and alkyl sulfone;
R 23选自芳基、杂芳基、-O-芳基、-O-杂芳基、-O-烷基、-O-烷基-环烷基、-NH-烷基、-NH-烷基-环烷基、-N(H)-芳基、-N(H)-杂芳基、-N(烷基)-芳基、-N(烷基)-杂芳基，所述芳基或杂芳基可以被卤素、C 1-C 6烷基、羟基化的C 1-C 6烷基、环烷基、氟取代的C 1-C 6烷基、CN、烷氧基、烷基砜、酰胺和磺酰胺取代； R 23 is selected from aryl, heteroaryl, -O-aryl, -O-heteroaryl, -O-alkyl, -O-alkyl-cycloalkyl, -NH-alkyl, -NH-alkane yl-cycloalkyl, -N(H)-aryl, -N(H)-heteroaryl, -N(alkyl)-aryl, -N(alkyl)-heteroaryl, the aryl Or heteroaryl can be halogen, C1 - C6 alkyl, hydroxylated C1 - C6 alkyl, cycloalkyl, fluorine substituted C1 - C6 alkyl, CN, alkoxy, alkyl Sulfone, amide and sulfonamide substitution;
R 24选自-CH 2-(C 1-C 6烷基)、-CH 2-环烷基、-CH 2-芳基、CH 2-杂芳基，其中烷基、环烷基、芳基和杂芳基可以被卤素、烷氧基、羟基化的烷基、氰基取代的烷基、环烷基和取代的环烷基取代； R 24 is selected from -CH 2 -(C 1 -C 6 alkyl), -CH 2 -cycloalkyl, -CH 2 -aryl, CH 2 -heteroaryl, wherein alkyl, cycloalkyl, aryl and heteroaryl can be substituted by halogen, alkoxy, hydroxylated alkyl, cyano-substituted alkyl, cycloalkyl and substituted cycloalkyl;
R 25选自C 1-C 6烷基，C 1-C 6烷基-环烷基，烷氧基取代的烷基，羟基化的烷基，芳基，杂芳基，取代的芳基或杂芳基，5、6和7元含氮饱和杂环，5,6-稠合和6,6-稠合的含氮饱和杂环，并且这些饱和杂环可以被C1-6烷基、氟取代的C 1-C 6烷基、烷氧基、芳基和杂芳基取代； R 25 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkyl-cycloalkyl, alkoxy substituted alkyl, hydroxylated alkyl, aryl, heteroaryl, substituted aryl or Heteroaryl, 5-, 6- and 7-membered nitrogen-containing saturated heterocycles, 5,6-fused and 6,6-fused nitrogen-containing saturated heterocycles, and these saturated heterocycles can be replaced by C1-6 alkyl, fluorine Substituted C1 - C6 alkyl, alkoxy, aryl and heteroaryl substitution;
R 26选自C 1-C 6烷基、C 3-C 6环烷基，所述烷基或环烷基可以被-OH、烷氧基、氟取代的烷氧基、氟取代的烷基、-NH 2、-NH-烷基、NH-C(O)烷基、-NH-S(O) 2-烷基和-S(O) 2-烷基取代； R 26 is selected from C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, and the alkyl or cycloalkyl may be -OH, alkoxy, fluorine-substituted alkoxy, fluorine-substituted alkyl , -NH2 , -NH-alkyl, NH-C(O)alkyl, -NH-S(O) 2 -alkyl and -S(O) 2 -alkyl substitution;
R 27选自芳基、杂芳基、双环杂芳基，其中所述芳基或杂芳基可以被C 1-C 6烷基、烷氧基、NH 2、NH-烷基、卤素或-CN取代，并且所述取代可以独立地是单取代、双取代和三取代； R 27 is selected from aryl, heteroaryl, bicyclic heteroaryl, wherein said aryl or heteroaryl may be represented by C 1 -C 6 alkyl, alkoxy, NH 2 , NH-alkyl, halogen or - CN substitution, and the substitution can independently be mono-, di-, and tri-substituted;
R 28选自芳基，5和6元杂芳基，双环杂芳基，环烷基，饱和杂环例如哌啶、哌啶酮、四氢吡喃、N-酰基-哌啶，其中所述环烷基、饱和杂环、芳基或杂芳基可以进一步被-OH，烷氧基，单取代、二取代或三取代基包括卤素、-CN、烷基砜和氟取代的烷基取代；和 R 28 is selected from aryl, 5 and 6 membered heteroaryl, bicyclic heteroaryl, cycloalkyl, saturated heterocycle such as piperidine, piperidone, tetrahydropyran, N-acyl-piperidine, wherein the Cycloalkyl, saturated heterocycle, aryl or heteroaryl can be further substituted with -OH, alkoxy, mono-, di- or tri-substituted including halogen, -CN, alkyl sulfone and fluorine substituted alkyl; and
R 1”选自烷基、芳基取代的烷基、烷氧基取代的烷基、环烷基、芳基取代的环烷基和烷氧基取代的环烷基。 R 1" is selected from alkyl, aryl-substituted alkyl, alkoxy-substituted alkyl, cycloalkyl, aryl-substituted cycloalkyl, and alkoxy-substituted cycloalkyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E28、E28a、E28b、E28c、E28d、E28e、E28f、E28g、E28h或E28i,(MDM2)The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of E28, E28a, E28b, E28c, E28d, E28e, E28f, E28g, E28h or E28i, (MDM2)
Figure PCTCN2022088560-appb-000440
Figure PCTCN2022088560-appb-000440
Figure PCTCN2022088560-appb-000441
Figure PCTCN2022088560-appb-000441
其中所述E28、E28a、E28b、E28c、E28d、E28e、E28f、E28g、E28h和E28i中：R 1’和R 2’各自独立的为F、Cl、Br、I、乙炔基、氰基、硝基或CF 3； Wherein said E28, E28a, E28b, E28c, E28d, E28e, E28f, E28g, E28h and E28i: R 1' and R 2' are independently F, Cl, Br, I, ethynyl, cyano, nitro base or CF 3 ;
R 3’选自-OCH 3、-OCH 2CH 3、-OCH 2CH 2F、-OCH 2CH 2OCH 3或-OCH(CH 3) 2； R 3' is selected from -OCH 3 , -OCH 2 CH 3 , -OCH 2 CH 2 F, -OCH 2 CH 2 OCH 3 or -OCH(CH 3 ) 2 ;
R 4’选自氢、卤素、甲基、-CF 3、-OCH 3、-C(CH 3) 3、-CH(CH 3) 2、-环丙基、氰基、-C(CH 3) 2OH、-C(CH 3) 2OCH 2CH 3、-C(CH 3) 2OCH 2OH、-C(CH 3) 2CH 2OCH 2CH 3、-C(CH 3) 2CH 2OCH 2CH 2OH、-C(CH 3) 2CN、-C(CH 3) 2C(O)CH 3、-C(CH 3) 2C(O)NHCH 3、-C(CH 3) 2C(O)N(CH 3) 2、-SCH 3、-SCH 2CH 3、-S(O) 2CH 3、-S(O) 2CH 2CH 3、-NHC(CH 3) 3、-NC(CH 3) 2、吡咯烷基或吗啉基； R 4' is selected from hydrogen, halogen, methyl, -CF 3 , -OCH 3 , -C(CH 3 ) 3 , -CH(CH 3 ) 2 , -cyclopropyl, cyano, -C(CH 3 ) 2 OH, -C(CH 3 ) 2 OCH 2 CH 3 , -C(CH 3 ) 2 OCH 2 OH, -C(CH 3 ) 2 CH 2 OCH 2 CH 3 , -C(CH 3 ) 2 CH 2 OCH 2 CH 2 OH, -C(CH 3 ) 2 CN, -C(CH 3 ) 2 C(O)CH 3 , -C(CH 3 ) 2 C(O)NHCH 3 , -C(CH 3 ) 2 C (O)N(CH 3 ) 2 , -SCH 3 , -SCH 2 CH 3 , -S(O) 2 CH 3 , -S(O) 2 CH 2 CH 3 , -NHC(CH 3 ) 3 , -NC (CH 3 ) 2, pyrrolidinyl or morpholinyl;
R 5’选自卤素、环丙基、-S(O) 2CH 3、-S(O) 2CH 2CH 3、吡咯烷基、-NH 2、-N(CH 3) 2或-NHC(CH 3) 3； R 5' is selected from halogen, cyclopropyl, -S(O) 2 CH 3 , -S(O) 2 CH 2 CH 3 , pyrrolidinyl, -NH 2 , -N(CH 3 ) 2 or -NHC ( CH 3 ) 3 ;
R 6’选自氢、
Figure PCTCN2022088560-appb-000442
Figure PCTCN2022088560-appb-000443
Figure PCTCN2022088560-appb-000444
或者
Figure PCTCN2022088560-appb-000445
其中R 6’中所述×为连接至L的连接点；或者R 4’也可连接至L； R 6' is selected from hydrogen,
Figure PCTCN2022088560-appb-000442
Figure PCTCN2022088560-appb-000443
Figure PCTCN2022088560-appb-000444
or
Figure PCTCN2022088560-appb-000445
wherein X described in R 6' is the point of attachment to L; or R 4' can also be attached to L;
R 7’为1个或多个卤素； R 7' is 1 or more halogen;
R 8’为1个或多个选自氢、F、Cl、Br、I、氰基、硝基、乙炔基、环丙基、甲基、乙基、异丙基、乙烯基、甲氧基、乙氧基、异丙氧基、羟基、其他的C 1-C 6烷基、其他的C 1-C 6烯基、其他的C 1-C 6炔基； R 8' is one or more selected from hydrogen, F, Cl, Br, I, cyano, nitro, ethynyl, cyclopropyl, methyl, ethyl, isopropyl, vinyl, methoxy , ethoxy, isopropoxy, hydroxyl, other C 1 -C 6 alkyl, other C 1 -C 6 alkenyl, other C 1 -C 6 alkynyl;
R 9’为任选取代的烷基、任选取代的烯基、任选取代的炔基、任选取代的芳基、任选取代的杂芳基、任选取代的环烷基； R 9' is optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl;
Z为氢、-OCH 3、-OCH 2CH 3或者卤素； Z is hydrogen, -OCH 3 , -OCH 2 CH 3 or halogen;
R 10’和 R11’各自独立的为氢、(CH 2) n-R’、(CH 2) n-NR’R”、(CH 2) n-NR’C(O)R”、(CH 2) n-NR’S(O) 2R”、(CH 2) n-C(O)OH、(CH 2) n-C(O)OR’、(CH 2) n-C(O)NR’R”、(CH 2) n-OR’、(CH 2) n-SR’、(CH 2) n-SOR’、(CH 2) n-CH(OH)-R’、(CH 2) n-C(O)R’、(CH 2) n-S(O) 2R’、(CH 2) n-S(O)NR’R”、(CH 2) n-S(O) 2NR’R”、(CH 2CH 2O) m-(CH 2) n-R’、(CH 2CH 2O) m-(CH 2) n-OH、 R 10' and R11' are each independently hydrogen, (CH 2 ) n -R', (CH 2 ) n -NR'R", (CH 2 ) n -NR'C(O)R", (CH 2 ) n -NR'S(O) 2 R", (CH 2 ) n -C(O)OH, (CH 2 ) n -C(O)OR', (CH 2 ) n -C(O)NR'R" , (CH 2 ) n -OR', (CH 2 ) n -SR', (CH 2 ) n -SOR', (CH 2 ) n -CH(OH)-R', (CH 2 ) n -C( O)R', (CH 2 ) n -S(O) 2 R', (CH 2 ) n -S(O)NR'R", (CH 2 ) n -S(O) 2 NR'R", (CH 2 CH 2 O) m -(CH 2 ) n -R', (CH 2 CH 2 O) m -(CH 2 ) n -OH,
(CH 2CH 2O) m-(CH 2) n-OR’、(CH 2CH 2O) m-(CH 2) n-NR’R”、(CH 2CH 2O) m-(CH 2) n-NR’C(O)R”、(CH 2CH 2O) m-(CH 2) n-S(O) 2NR’R”、(CH 2CH 2O) m-(CH 2) n-C(O)OH、(CH 2CH 2O) m-(CH 2) n-C(O)OR’、(CH 2CH 2O) m-(CH 2) n-C(O)NR’R”、(CH 2CH 2O) m-(CH 2) n-S(O)OR’、(CH 2CH 2O) m-(CH 2) n-C(O)R’、(CH 2CH 2O) m-(CH 2) n-S(O)NR’R”、(CH 2CH 2O) m-(CH 2) n-S(O) 2NR’R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) nR’、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-OH、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-OR’、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-NR’R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-NR’C(O)R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-NR’S(O) 2R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-C(O)OH、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-C(O)OR’、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-C(O)NR’R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-S(O) 2R’、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-C(O)R’、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-S(O)NR’R”、-(CH 2) p-(CH 2CH 2O) m-(CH 2) n-S(O) 2NR’R”、芳基-(CH 2) n-C(O)OH或杂芳基-烷基-C(O)-烷基-NR’R”，所述烷基任选被OR’取代；或者R 10’和R 11’各自独立的为杂芳基-(CH2)n-杂环烷基，所述杂环烷基任选的烷基、羟基、C(O)OR’或者C(O)R’取代；所述R’和R”各自独立的选自氢、任选被选自卤素、羟基、NH 2、NH(烷基)、NH(烷基) 1-2、氧代、羧基、环烷基或者杂芳基； (CH 2 CH 2 O) m -(CH 2 ) n -OR', (CH 2 CH 2 O) m -(CH 2 ) n -NR'R”, (CH 2 CH 2 O) m -(CH 2 ) n -NR'C(O)R", (CH 2 CH 2 O) m -(CH 2 ) n -S(O) 2 NR'R", (CH 2 CH 2 O) m -(CH 2 ) n- C(O)OH, (CH 2 CH 2 O) m -(CH 2 ) n -C(O)OR', (CH 2 CH 2 O) m -(CH 2 ) n -C(O)NR 'R', (CH 2 CH 2 O) m -(CH 2 ) n -S(O)OR', (CH 2 CH 2 O) m -(CH 2 ) n -C(O)R', (CH 2 2 CH 2 O) m -(CH 2 ) n -S(O)NR'R", (CH 2 CH 2 O) m -(CH 2 ) n -S(O) 2 NR'R", -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n R', -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -OH, -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -OR', -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -NR'R”, -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -NR'C(O)R", -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n - NR'S(O) 2 R", -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -C(O)OH, -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -C(O)OR', -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -C(O)NR'R", -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -S(O) 2 R', -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -C( O)R', -(CH 2 ) p -(CH 2 CH 2 O) m -(CH 2 ) n -S(O)NR'R", -(CH 2 ) p -(CH 2 CH 2 O) m- ( CH2 ) n -S(O)2NR'R", aryl-( CH2 ) n -C(O)OH or heteroaryl-alkyl-C(O)-alkyl-NR'R", said alkyl is optionally substituted by OR'; or R 10' and R 11' are each independently heteroaryl-(CH2)n-heterocycloalkyl, and said heterocycloalkyl is optionally alkane group, hydroxyl, C(O)OR' or C(O)R'substituted; said R' and R" are each independently selected from hydrogen, optionally selected from halogen, hydroxyl, NH2 , NH(alkyl) , NH(alkyl) 1-2 , oxo, carboxyl, cycloalkyl or heteroaryl;
m、n和p各自独立的为0、1、2、3、4、5或者6；m, n, and p are each independently 0, 1, 2, 3, 4, 5, or 6;
R 12’各自独立的为-O-烷基、-O-烷基-烷氧基、-C(O)-烷基、-C(OH)-烷基-烷氧基、-C(O)-NH-烷基、-C(O)-N-(烷基) 1-2、-S(O)-烷基、S(O) 2-烷基、-C(O)-环胺、-O-芳基-烷基、-O-芳基-烷氧基； R 12' is each independently -O-alkyl, -O-alkyl-alkoxy, -C(O)-alkyl, -C(OH)-alkyl-alkoxy, -C(O) -NH-alkyl, -C(O)-N-(alkyl) 1-2 , -S(O)-alkyl, S(O) 2 -alkyl, -C(O)-cyclic amine, - O-aryl-alkyl, -O-aryl-alkoxy;
R 1”选自氢、任选被芳基或烷氧基取代的烷基、任选被芳基或者烷氧基取代的环烷基。 R1 " is selected from hydrogen, alkyl optionally substituted with aryl or alkoxy, cycloalkyl optionally substituted with aryl or alkoxy.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E29：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E29:
Figure PCTCN2022088560-appb-000446
Figure PCTCN2022088560-appb-000446
R 1独立地选自H、C 1-C 4-烷基、C 1-C 4-烯基、C 1-C 4-炔基或C 3-C 10-环烷基，其是未被取代或被取代的； R 1 is independently selected from H, C 1 -C 4 -alkyl, C 1 -C 4 -alkenyl, C 1 -C 4 -alkynyl or C 3 -C 10 -cycloalkyl, which is unsubstituted or replaced;
R 2独立地选自H、C 1-C 4-烯基、C 1-C 4-烯基、C 1-C 4-炔基或C 3-C 10-环烷基，其是未被取代或被取代的； R 2 is independently selected from H, C 1 -C 4 -alkenyl, C 1 -C 4 -alkenyl, C 1 -C 4 -alkynyl or C 3 -C 10 -cycloalkyl, which is unsubstituted or replaced;
R 3独立地选自H、-CF 3、-C 2H 5、C 1-C 4-烷基、C 1-C 4-烯基、C 1-C 4-炔基、-CH 2-Z或任一R 2和R 3一起形成杂环； R 3 is independently selected from H, -CF 3 , -C 2 H 5 , C 1 -C 4 -alkyl, C 1 -C 4 -alkenyl, C 1 -C 4 -alkynyl, -CH 2 -Z Or any R 2 and R 3 together form a heterocycle;
每个Z独立地选自H、-OH、F、Cl、-CH 3、-CF 3、-CH 2Cl、-CH 2F或-CH 2OH； each Z is independently selected from H, -OH, F, Cl, -CH3 , -CF3 , -CH2Cl , -CH2F, or -CH2OH ;
R 4独立地选自C 1-C 16直链或支链烷基、C 1-C 16-烯基、C 1-C 16-炔基、C 3-C 10-环烷基、-(CH 2) 0-6-Z 1、-(CH 2) 0- 6-芳基和-(CH 2) 0-6-het，其中烷基、环烷基和苯基未被取代或被取代； R 4 is independently selected from C 1 -C 16 straight or branched chain alkyl, C 1 -C 16 -alkenyl, C 1 -C 16 -alkynyl, C 3 -C 10 -cycloalkyl, -(CH 2 ) 0-6 - Z1, -(CH2)0-6-aryl and -(CH2)0-6 - het , wherein alkyl, cycloalkyl and phenyl are unsubstituted or substituted;
R 5独立地选自H、C 1-10-烷基、芳基、苯基、C 3-7-环烷基、-(CH 2) 1-6-C 3-7-环烷基、-C 1-10-烷基-芳基、-(CH 2) 0-6-C 3-7-环烷基-(CH 2) 0-6-苯基、-(CH 2) 0-4-CH[(CH 2) 1-4-苯基] 2、茚满基、-C(O)-C 1-10-烷基、-C(O)-(CH 2) 1- 6-C 3-7-环烷基、-C(O)-(CH 2) 0-6-苯基、-(CH 2) 0-6-C(O)-苯基、-(CH 2) 0-6-het、-C(O)-(CH 2) 1-6-het或R 5选自氨基酸的残基，其中烷基、环烷基、苯基和芳基取代基未被取代或被取代； R 5 is independently selected from H, C 1-10 -alkyl, aryl, phenyl, C 3-7 -cycloalkyl, -(CH 2 ) 1-6 -C 3-7 -cycloalkyl, - C1-10 -Alkyl-aryl, -( CH2 ) 0-6 - C3-7 -cycloalkyl-( CH2 ) 0-6 -phenyl, -( CH2 ) 0-4 -CH [(CH 2 ) 1-4 -phenyl] 2 , indanyl, -C(O)-C 1-10 -alkyl, -C(O)-(CH 2 ) 1- 6 -C 3-7 -Cycloalkyl, -C(O)-( CH2 ) 0-6 -phenyl, -( CH2 ) 0-6 -C(O)-phenyl, -( CH2 ) 0-6 -het, -C(O)-( CH2 ) 1-6 - het or R5 is selected from the residues of amino acids in which the alkyl, cycloalkyl, phenyl and aryl substituents are unsubstituted or substituted;
Z 1独立地选自-N(R 10)-C(O)-C 1-10-烷基、-N(R 10)-C(O)-(CH 2) 0-6-C 3-7-环烷基、-N(R 10)-C(O)-(CH 2) 0-6-苯基、-N(R 10)-C(O)(CH 2) 1-6-het、-C(O)-N(R 11)(R 12)、-C(O)-O-C 1-10-烷基、-C(O)-O-(CH 2) 1-6-C 3-7-环烷基、-C(O)-O-(CH 2) 0-6-苯基、-C(O)-O-(CH 2) 1-6-het、-O-C(O)-C 1-10-烷基、-O-C(O)-(CH 2) 1-6-C 3-7-环烷基、-O-C(O)-(CH 2) 0-6-苯基、-O-C(O)-(CH 2) 1-6-het，其中烷基、环烷基和苯基未被取代或被取代； Z 1 is independently selected from -N(R 10 )-C(O)-C 1-10 -alkyl, -N(R 10 )-C(O)-(CH 2 ) 0-6 -C 3-7 -Cycloalkyl, -N(R10)-C(O) - ( CH2 ) 0-6 -phenyl, -N(R10)-C(O)( CH2 ) 1-6 -het, - C(O)-N(R 11 )(R 12 ), -C(O)-OC 1-10 -Alkyl, -C(O)-O-(CH 2 ) 1-6 -C 3-7 - Cycloalkyl, -C(O)-O-(CH 2 ) 0-6 -phenyl, -C(O)-O-(CH 2 ) 1-6 -het, -OC(O)-C 1- 10 -Alkyl, -OC(O)-(CH 2 ) 1-6 -C 3-7 -cycloalkyl, -OC(O)-(CH 2 ) 0-6 -phenyl, -OC(O) -( CH2 ) 1-6 -het, wherein alkyl, cycloalkyl and phenyl are unsubstituted or substituted;
het独立地选自含有1-4个选自N、O和S的杂原子的5-7元杂环或8-12元稠合环系，其包括至少一个含有1、2或3个选自N、O和S的杂原子的5-7元杂环，所述杂环或稠合环系在碳或氮原子上未被取代或被取代；het is independently selected from 5-7 membered heterocycles or 8-12 membered fused ring systems containing 1-4 heteroatoms selected from N, O and S, including at least one member containing 1, 2 or 3 heteroatoms selected from 5-7 membered heterocycles of heteroatoms of N, O and S which are unsubstituted or substituted on carbon or nitrogen atoms;
R 10选自H、-CH 3、-CF 3、-CH 2OH或-CH 2Cl； R 10 is selected from H, -CH 3 , -CF 3 , -CH 2 OH or -CH 2 Cl;
R 11和R 12独立地选自H、C 1-4-烷基、C 3-7-环烷基、-(CH 2) 1-6-C 3-7-环烷基、(CH 2) 0-6-苯基，其中烷基、环烷基和苯基未被取代或被取代；或R 11和R 12与氮一起形成het，并且 R 11 and R 12 are independently selected from H, C 1-4 -alkyl, C 3-7 -cycloalkyl, -(CH 2 ) 1-6 -C 3-7 -cycloalkyl, (CH 2 ) 0-6 -phenyl, wherein alkyl, cycloalkyl and phenyl are unsubstituted or substituted; or R and R together with nitrogen form het , and
U独立地为：U is independently:
Figure PCTCN2022088560-appb-000447
Figure PCTCN2022088560-appb-000447
其中：in:
每个n独立地选自0-5；each n is independently selected from 0-5;
X选自-CH和N；X is selected from -CH and N;
R a和R b独立地选自O、S或N原子或C 0-8-烷基，其中烷基链中的一个或多个碳原子任选被选自O、S或N的杂原子替代，并且其中每个烷基独立地未被取代或被取代； Ra and Rb are independently selected from O, S or N atoms or Co- 8 -alkyl, wherein one or more carbon atoms in the alkyl chain are optionally replaced by heteroatoms selected from O, S or N , and wherein each alkyl group is independently unsubstituted or substituted;
R d选自Re-Q-(R f) p(R g) q和Ar 1-D-Ar 2； R d is selected from Re-Q-(R f ) p (R g ) q and Ar 1 -D-Ar 2 ;
R c选自H或任一R c和R d一起形成环烷基或het；其中如果R c和R d形成环烷基或het，则R 5在C或N原子处连接至形成的环； R is selected from H or either R and R together form a cycloalkyl or het ; wherein if R and R form a cycloalkyl or het , then R is attached to the formed ring at a C or N atom ;
p和q独立地选自0或1；p and q are independently selected from 0 or 1;
R e选自C 1-8-烷基和亚烷基，并且每个R e未被取代或被取代； R e is selected from C 1-8 -alkyl and alkylene, and each R e is unsubstituted or substituted;
Q选自N、O、S、S(O)和S(O) 2； Q is selected from N, O, S, S(O) and S(O) 2 ;
Ar 1和Ar 2独立地选自被取代或未被取代的芳基和het； Ar 1 and Ar 2 are independently selected from substituted or unsubstituted aryl and het;
R f和R g独立地选自H、-C 1- 10-烷基、C 1-10-烷基芳基、-OH、-O-C 1-10-烷基、-(CH 2) 0-6-C 3-7-环烷基、-O-(CH 2) 0-6-芳基、苯基、芳基、苯基-苯基、-(CH 2) 1-6-het、-O-(CH 2) 1-6-het、-OR 13、-C(0)-R 13、-C(O)-N(R 13)(R 14)、-N(R 13)(R 14)、-S-R 13、-S(O)-R 13、-S(O) 2-R 13、-S(O) 2-NR 13R 14、-NR 13-S(O) 2-R 14、-S-C t-10-烷基、芳基-C 1-4-烷基或het-C 1-4-烷基，其中烷基、环烷基、het和芳基未被取代或被取代，-SO 2-C 1-2-烷基、-SO 2-C 1-2-烷基苯基、-O-C 1-4-烷基或任一R g和R f一起形成选自het或芳基的环； R f and R g are independently selected from H, -C 1-10 -alkyl, C 1-10 -alkylaryl , -OH, -OC 1-10 -alkyl, -(CH 2 ) 0-6 -C3-7 -cycloalkyl, -O-( CH2 ) 0-6 -aryl, phenyl, aryl, phenyl-phenyl, -( CH2 ) 1-6 -het, -O- (CH 2 ) 1-6 -het, -OR 13 , -C(0)-R 13 , -C(O)-N(R 13 )(R 14 ), -N(R 13 )(R 14 ), -SR 13 , -S(O)-R 13 , -S(O) 2 -R 13 , -S(O) 2 -NR 13 R 14 , -NR 13 -S(O) 2 -R 14 , -SC t-10 -Alkyl, aryl-C 1-4 -alkyl or het-C 1-4 -alkyl, wherein alkyl, cycloalkyl, het and aryl are unsubstituted or substituted, -SO 2 -C 1-2 -alkyl, -SO 2 -C 1-2 -alkylphenyl, -OC 1-4 -alkyl or any of R g and R f taken together to form a ring selected from het or aryl;
D选自-CO-、-C(O)-C 1-7-亚烷基或亚芳基、-CF 2-、-O-、-S(O) r，其中r是0-2、1,3-二氧杂环戊烷或C 1- 7-烷基-OH；其中烷基、亚烷基或亚芳基未被取代或被一个或多个卤素、OH、-O-C 1-6-烷基、-S-C 1-6-烷基或-CF 3取代；或每个D独立地选自N(R h)； D is selected from -CO-, -C(O)-Ci- 7 -alkylene or arylene, -CF2- , -O-, -S(O) r , wherein r is 0-2, 1 , 3-dioxolane or C 1-7 -alkyl-OH; wherein alkyl, alkylene or arylene is unsubstituted or replaced by one or more halogens, OH, -OC 1-6 - Alkyl, -SC 1-6 -alkyl or -CF 3 substituted; or each D is independently selected from N(R h );
R h选自H、未被取代或被取代的C 1-7-烷基、芳基、未被取代或被取代的-O-(C 1-7-环烷基)、-C(O)-C 1-10-烷基、-C(O)-C 0-10-烷基-芳基、-C-O-C 01-10-烷基、-C-O-C 0-10-烷基-芳基、-SO 2-C 1-10-烷基或-SO 2-(C 0-10-烷基芳基)； R h is selected from H, unsubstituted or substituted C 1-7 -alkyl, aryl, unsubstituted or substituted -O-(C 1-7 -cycloalkyl), -C(O) -C 1-10 -alkyl, -C(O)-C 0-10 -alkyl-aryl, -COC 01-10 -alkyl, -COC 0-10 -alkyl-aryl, -SO 2 -C 1-10 -alkyl or -SO 2 -(C 0-10 -alkylaryl );
R 6、R 7、R 8和R 9独立地选自H、-C 1-10-烷基、-C 1-10-烷氧基、芳基-C 1-10-烷氧基、-OH、-O-C 1-10-烷基、-(CH 2) 0-6-C 3-7-环烷基、-O-(CH 2) 0-6-芳基、苯基、-(CH 2) 1-6-het、-O-(CH 2) 1-6-het、-OR 13、-C(O)-R 13、-C(O)-N(R 13)(R 14)、-N(R 13)(R 14)、-S-R 13、-S(O)-R 13、-S(O) 2-R 13、-S(O) 2-NR 13R 14或-NR 13-S(O) 2-R 14；其中每个烷基、环烷基和芳基未被取代或被取代；并且任一R 6、R 7、R 8和R 9任选一起形成环系； R 6 , R 7 , R 8 and R 9 are independently selected from H, -C 1-10 -alkyl, -C 1-10 -alkoxy, aryl-C 1-10 -alkoxy, -OH , -OC 1-10 -alkyl, -(CH 2 ) 0-6 -C 3-7 -cycloalkyl, -O-(CH 2 ) 0-6 -aryl, phenyl, -(CH 2 ) 1-6 -het, -O-(CH 2 ) 1-6 -het, -OR 13 , -C(O)-R 13 , -C(O)-N(R 13 )(R 14 ), -N (R 13 )(R 14 ), -SR 13 , -S(O)-R 13 , -S(O) 2 -R 13 , -S(O) 2 -NR 13 R 14 or -NR 13 -S( O) 2 -R 14 ; wherein each alkyl, cycloalkyl and aryl group is unsubstituted or substituted; and any of R 6 , R 7 , R 8 and R 9 are optionally taken together to form a ring system;
R 13和R 14独立地选自H、C 1-10-烷基、-(CH 2) 0-6-C 3-7-环烷基、-(CH 2) 0-6-(CH) 0-1-(芳基) 1-2、-C(O)-C 1-10-烷基、-C(O)-(CH 2) 1-6-C 3-7-环烷基、-C(O)-O-(CH 2) 0-6-芳基、-C(O)-(CH 2) 0-6-O-芴基、-C(O)-NH-(CH 2) 0-6-芳基、-C(O)-(CH 2) 0-6-芳基、-C(O)-(CH 2) 0-6-het、-C(S)-C 1-10-烷基、-C(S)-(CH 2) 1-6-C 3-7-环烷基、-C(S)-O-(CH 2) 0-6-芳基、-C(S)-(CH 2) 0-6-O-芴基、-C(S)-NH-(CH 2) 0-6-芳基、-C(S)-(CH 2) 0-6-芳基或-C(S)-(CH 2) 1-6-het，其中每个烷基、环烷基和芳基未被取代或被取代；或任一R 13和R 14与氮原子一起形成het； R 13 and R 14 are independently selected from H, C 1-10 -alkyl, -(CH 2 ) 0-6 -C 3-7 -cycloalkyl, -(CH 2 ) 0-6 -(CH) 0 -1 -(aryl) 1-2 , -C(O)-C 1-10 -alkyl, -C(O)-(CH 2 ) 1-6 -C 3-7 -cycloalkyl, -C (O)-O-(CH 2 ) 0-6 -aryl, -C(O)-(CH 2 ) 0-6 -O-fluorenyl, -C(O)-NH-(CH 2 ) 0- 6 -Aryl, -C(O)-( CH2 ) 0-6 -aryl, -C(O)-( CH2 ) 0-6 -het, -C(S) -C1-10 -alkane group, -C(S)-(CH 2 ) 1-6 -C 3-7 -cycloalkyl, -C(S)-O-(CH 2 ) 0-6 -aryl, -C(S)- (CH 2 ) 0-6 -O-fluorenyl, -C(S)-NH-(CH 2 ) 0-6 -aryl, -C(S)-(CH 2 ) 0-6 -aryl or - C(S)-( CH2 ) 1-6 -het, wherein each alkyl, cycloalkyl and aryl group is unsubstituted or substituted; or any of R13 and R14 are taken together with the nitrogen atom to form het;
R 13和R 14的烷基取代基未被取代或被取代，并且当被取代时，被一个或多个取代基取代，所述取代基选自C 1-10-烷基、卤素、OH、-O-C 1-6-烷基、-S-C 1-6-烷基和-CF 3；并且R 13和R 14的取代的苯基或芳基被一个或多个取代基取代，所述取代基选自卤素、羟基、C 1-4-烷基、C 1-4-烷氧基、硝基、-CN、-O-C(O)-C 1-4-烷基和-C(O)-O-C 1-4-芳基；或其药学上可接受的盐或水合物。 The alkyl substituents of R 13 and R 14 are unsubstituted or substituted, and when substituted, are substituted with one or more substituents selected from C 1-10 -alkyl, halogen, OH, -OC 1-6 -alkyl, -SC 1-6 -alkyl and -CF 3 ; and the substituted phenyl or aryl of R 13 and R 14 is substituted with one or more substituents, the substituents being selected from From halogen, hydroxyl, C1-4 -alkyl, C1-4 -alkoxy, nitro, -CN, -OC(O) -C1-4 -alkyl and -C(O) -OC1 -4 -aryl; or a pharmaceutically acceptable salt or hydrate thereof.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E30、E30a、E30b、E30c或E30d：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E30, E30a, E30b, E30c or E30d:
Figure PCTCN2022088560-appb-000448
Figure PCTCN2022088560-appb-000448
Figure PCTCN2022088560-appb-000449
Figure PCTCN2022088560-appb-000449
其中E30、E30a、E30b、E30c和E30d中：Among them E30, E30a, E30b, E30c and E30d:
R 1选自氢或者烷基； R 1 is selected from hydrogen or alkyl;
R 2选自氢或者烷基； R 2 is selected from hydrogen or alkyl;
R 3选自氢、烷基、环烷基或杂环烷基； R is selected from hydrogen, alkyl, cycloalkyl or heterocycloalkyl;
R 5和R 6各自独立的选自氢、烷基、环烷基或者杂环烷基；或者R 5、R 6与其所连接的原子一起形成吡咯烷基或哌啶环且任选的与1-2个环烷基、杂环烷基、芳基或者杂芳基环稠合，且所述每个环进一步任选的酬合至另外一个环烷基、杂环烷基、芳基或者杂芳基环； R 5 and R 6 are each independently selected from hydrogen, alkyl, cycloalkyl or heterocycloalkyl; or R 5 , R 6 together with the atoms to which they are attached form a pyrrolidinyl or piperidine ring and are optionally combined with 1 - 2 cycloalkyl, heterocycloalkyl, aryl or heteroaryl rings are fused, and each of said rings is further optionally fused to another cycloalkyl, heterocycloalkyl, aryl or heterocycle aryl ring;
或者R 5和R 3与其所连接的原子一起形成5-8元环且任选的与1个或者2个环烷基、杂环烷基、芳基、杂芳基环酬合； Or R 5 and R 3 together with the atoms to which they are attached form a 5-8 membered ring and are optionally combined with 1 or 2 cycloalkyl, heterocycloalkyl, aryl, heteroaryl cyclic ketones;
R 4选自烷基、环烷基、杂环烷基、环烷基烷基、咋环烷基烷基、芳基或者双环芳基、芳基烷基、杂芳基或者双环杂芳基或杂芳基烷基，且进一步任选的被1-3个烷基、环烷基、杂环烷基、环烷基烷基、咋环烷基烷基、芳基或者双环芳基、芳基烷基、杂芳基或者双环杂芳基、杂芳基烷基取代基所取代。 R4 is selected from alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, azcycloalkylalkyl , aryl or bicyclic aryl, arylalkyl, heteroaryl or bicyclic heteroaryl or Heteroarylalkyl, and further optionally by 1-3 alkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, azcycloalkylalkyl, aryl or bicyclic aryl, aryl Alkyl, heteroaryl or bicyclic heteroaryl, heteroarylalkyl substituents.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E31The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E31
Figure PCTCN2022088560-appb-000450
Figure PCTCN2022088560-appb-000450
其中所述E31中：A1和A2各自独立地选自任选被取代的单环、稠环、芳基和杂芳基；wherein in said E31: A1 and A2 are each independently selected from optionally substituted monocyclic, fused ring, aryl and heteroaryl;
R选自H或Me。R is selected from H or Me.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E32,The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E32,
Figure PCTCN2022088560-appb-000451
Figure PCTCN2022088560-appb-000451
其中所述E32中：Where the E32:
R 1选自烷基、环烷基和杂环烷基，且最优选选自异丙基、叔丁基、环己基和四氢吡喃基；R 2选自–OPh或H。 R1 is selected from alkyl, cycloalkyl and heterocycloalkyl, and most preferably is selected from isopropyl, tert - butyl, cyclohexyl and tetrahydropyranyl; R2 is selected from -OPh or H.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E33,The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E33,
Figure PCTCN2022088560-appb-000452
Figure PCTCN2022088560-appb-000452
其中，所述E33中：Among them, in the E33:
R 1选自H、–CH 2OH、-CH 2CH 2OH、-CH 2NH 2、-CH 2CH 2NH 2； R 1 is selected from H, -CH 2 OH, -CH 2 CH 2 OH, -CH 2 NH 2 , -CH 2 CH 2 NH 2 ;
X选自S或CH 2； X is selected from S or CH 2 ;
n为1、2或者3；n is 1, 2 or 3;
R 2选自：
Figure PCTCN2022088560-appb-000453
R 2 is selected from:
Figure PCTCN2022088560-appb-000453
R 3和R 4独立地选自H或Me。 R3 and R4 are independently selected from H or Me.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E34，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E34,
Figure PCTCN2022088560-appb-000454
Figure PCTCN2022088560-appb-000454
其中所述E34中：Among them the E34:
R 1选自H或Me； R 1 is selected from H or Me;
R 2选自H或
Figure PCTCN2022088560-appb-000455
R 2 is selected from H or
Figure PCTCN2022088560-appb-000455
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E35，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E35,
Figure PCTCN2022088560-appb-000456
Figure PCTCN2022088560-appb-000456
其中所述E35中：Among them the E35:
R 1选自：
Figure PCTCN2022088560-appb-000457
R1 is selected from :
Figure PCTCN2022088560-appb-000457
R 2选自：
Figure PCTCN2022088560-appb-000458
R 2 is selected from:
Figure PCTCN2022088560-appb-000458
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E36，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E36,
Figure PCTCN2022088560-appb-000459
Figure PCTCN2022088560-appb-000459
其中所述E36中：Among them the E36:
n为0、1或者2，优选为2；n is 0, 1 or 2, preferably 2;
Z不存在或为O；Z does not exist or is O;
R 1选自： R1 is selected from :
Figure PCTCN2022088560-appb-000460
Figure PCTCN2022088560-appb-000460
Figure PCTCN2022088560-appb-000461
中的R 10选自氢、烷基或者芳基；
Figure PCTCN2022088560-appb-000461
R 10 in is selected from hydrogen, alkyl or aryl;
X选自CH 2和O；并且 X is selected from CH and O; and
Figure PCTCN2022088560-appb-000462
是含氮杂芳基。
Figure PCTCN2022088560-appb-000462
is a nitrogen-containing heteroaryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E37，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E37,
Figure PCTCN2022088560-appb-000463
Figure PCTCN2022088560-appb-000463
其中所述E37中：Among them the E37:
Z不存在或为O；Z does not exist or is O;
R 3和R 4独立地选自H或Me； R and R are independently selected from H or Me ;
R 1选自： R1 is selected from :
Figure PCTCN2022088560-appb-000464
Figure PCTCN2022088560-appb-000464
Figure PCTCN2022088560-appb-000465
中的R 10选自H、烷基或芳基；
Figure PCTCN2022088560-appb-000465
R 10 in is selected from H, alkyl or aryl;
Figure PCTCN2022088560-appb-000466
中的X选自CH 2和O；并且
Figure PCTCN2022088560-appb-000466
where X is selected from CH and O; and
Figure PCTCN2022088560-appb-000467
中的
Figure PCTCN2022088560-appb-000468
是含氮杂芳基。
Figure PCTCN2022088560-appb-000467
middle
Figure PCTCN2022088560-appb-000468
is a nitrogen-containing heteroaryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E38，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E38,
Figure PCTCN2022088560-appb-000469
Figure PCTCN2022088560-appb-000469
其中所述E38中：Among them the E38:
Z不存在或为O；Z does not exist or is O;
R 1选自： R1 is selected from :
Figure PCTCN2022088560-appb-000470
Figure PCTCN2022088560-appb-000470
Figure PCTCN2022088560-appb-000471
中的R 10选自H、烷基或芳基；
Figure PCTCN2022088560-appb-000471
R 10 in is selected from H, alkyl or aryl;
Figure PCTCN2022088560-appb-000472
中的X选自CH 2和O；并且
Figure PCTCN2022088560-appb-000472
where X is selected from CH and O; and
Figure PCTCN2022088560-appb-000473
中的
Figure PCTCN2022088560-appb-000474
是含氮杂芳基；并且
Figure PCTCN2022088560-appb-000473
middle
Figure PCTCN2022088560-appb-000474
is a nitrogen-containing heteroaryl; and
R 2选自H、烷基或酰基。 R 2 is selected from H, alkyl or acyl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E39，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E39,
Figure PCTCN2022088560-appb-000475
Figure PCTCN2022088560-appb-000475
其中所述E39中：Among them the E39:
R 2选自烷基、环烷基和杂环烷基；更优选地选自异丙基、叔丁基、环己基和四氢吡喃基，最优选地选自环己基； R 2 is selected from alkyl, cycloalkyl and heterocycloalkyl; more preferably from isopropyl, tert-butyl, cyclohexyl and tetrahydropyranyl, most preferably from cyclohexyl;
Figure PCTCN2022088560-appb-000476
是5-或6-元含氮杂芳基；更优选5-元含氮杂芳基并且最优选噻唑；并且
Figure PCTCN2022088560-appb-000476
is a 5- or 6-membered nitrogen-containing heteroaryl; more preferably a 5-membered nitrogen-containing heteroaryl and most preferably a thiazole; and
Ar是芳基或杂芳基。Ar is aryl or heteroaryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E40，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of , E is E40,
Figure PCTCN2022088560-appb-000477
Figure PCTCN2022088560-appb-000477
其中所述E40中：Among them the E40:
R 1选自卤素(例如，氟)、氰基、
Figure PCTCN2022088560-appb-000478
R 1 is selected from halogen (eg, fluorine), cyano,
Figure PCTCN2022088560-appb-000478
X选自O或CH 2。 X is selected from O or CH2 .
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E41，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E41,
Figure PCTCN2022088560-appb-000479
Figure PCTCN2022088560-appb-000479
其中，所述E41中：Among them, in the E41:
R选自烷基、芳基、杂芳基、芳基烷基、杂芳基烷基或卤素(在可变取代位置中)。R is selected from alkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl or halogen (in variable substitution positions).
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E42，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E42,
Figure PCTCN2022088560-appb-000480
Figure PCTCN2022088560-appb-000480
其中所述E36中，
Figure PCTCN2022088560-appb-000481
是6-元含氮杂芳基。 wherein the E36,
Figure PCTCN2022088560-appb-000481
is a 6-membered nitrogen-containing heteroaryl.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E43，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E43,
Figure PCTCN2022088560-appb-000482
Figure PCTCN2022088560-appb-000482
其中，所述E43中，X选自CH 2、O、NH或S。 Wherein, in the E43, X is selected from CH 2 , O, NH or S.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E44、E44a或E44b,The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E44, E44a or E44b,
Figure PCTCN2022088560-appb-000483
Figure PCTCN2022088560-appb-000483
其中所述E44、E44a和E44b中：wherein said E44, E44a and E44b:
n为1或2；n is 1 or 2;
R 2、R 3和R 4独立地选自H或甲基； R 2 , R 3 and R 4 are independently selected from H or methyl;
X独立地选自O或S；X is independently selected from O or S;
并且and
R 1选自： R1 is selected from :
Figure PCTCN2022088560-appb-000484
Figure PCTCN2022088560-appb-000484
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E45,The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E45,
Figure PCTCN2022088560-appb-000485
Figure PCTCN2022088560-appb-000485
其中所述E45中：Among them the E45:
R 3和R 4各自独立的选自氢或者甲基； R 3 and R 4 are each independently selected from hydrogen or methyl;
Figure PCTCN2022088560-appb-000486
为选自以下的5元杂环：
Figure PCTCN2022088560-appb-000487
或者
Figure PCTCN2022088560-appb-000488
Figure PCTCN2022088560-appb-000486
is a 5-membered heterocycle selected from:
Figure PCTCN2022088560-appb-000487
or
Figure PCTCN2022088560-appb-000488
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为E46或E46a，The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is E46 or E46a,
Figure PCTCN2022088560-appb-000489
Figure PCTCN2022088560-appb-000489
其中：in:
R 1选自：
Figure PCTCN2022088560-appb-000490
R1 is selected from :
Figure PCTCN2022088560-appb-000490
R 2选自H或甲基 R 2 is selected from H or methyl
n选自0、1或2。n is selected from 0, 1 or 2.
本发明式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐的一个优选实施方案中，E为：The compounds of formula I of the present invention, and/or their stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or their pharmaceutically acceptable salts In a preferred embodiment of, E is:
CRBN：CRBN:
Figure PCTCN2022088560-appb-000491
Figure PCTCN2022088560-appb-000491
VHL：VHL:
Figure PCTCN2022088560-appb-000492
Figure PCTCN2022088560-appb-000492
Figure PCTCN2022088560-appb-000493
Figure PCTCN2022088560-appb-000493
MDMA:MDMA:
Figure PCTCN2022088560-appb-000494
Figure PCTCN2022088560-appb-000494
IAP:IAP:
Figure PCTCN2022088560-appb-000495
Figure PCTCN2022088560-appb-000495
Figure PCTCN2022088560-appb-000496
Figure PCTCN2022088560-appb-000496
Figure PCTCN2022088560-appb-000497
Figure PCTCN2022088560-appb-000497
优选的，本发明某些实施方式中，所述式Ⅰ化合物为：Preferably, in some embodiments of the present invention, the compound of formula I is:
Figure PCTCN2022088560-appb-000498
Figure PCTCN2022088560-appb-000498
Figure PCTCN2022088560-appb-000499
Figure PCTCN2022088560-appb-000499
Figure PCTCN2022088560-appb-000500
Figure PCTCN2022088560-appb-000500
Figure PCTCN2022088560-appb-000501
Figure PCTCN2022088560-appb-000501
Figure PCTCN2022088560-appb-000502
Figure PCTCN2022088560-appb-000502
Figure PCTCN2022088560-appb-000503
Figure PCTCN2022088560-appb-000503
Figure PCTCN2022088560-appb-000504
Figure PCTCN2022088560-appb-000504
Figure PCTCN2022088560-appb-000505
Figure PCTCN2022088560-appb-000505
优选的，本发明某些实施方式中，所述式Ⅰ化合物为：Preferably, in some embodiments of the present invention, the compound of formula I is:
Figure PCTCN2022088560-appb-000506
Figure PCTCN2022088560-appb-000506
Figure PCTCN2022088560-appb-000507
Figure PCTCN2022088560-appb-000507
Figure PCTCN2022088560-appb-000508
Figure PCTCN2022088560-appb-000508
Figure PCTCN2022088560-appb-000509
Figure PCTCN2022088560-appb-000509
在某些实施方案中，所述氘代化物是化合物结构(例如L，例如LA、LA-1、LA-2、LA-3、LA-4、LA-5中的环A、环B、L 3、环C)中的1、2、3、4、5、6、7、8、9或10个H被氘替代形成的结构。在某些实施方案中，氘代的LA结构为
Figure PCTCN2022088560-appb-000510
Figure PCTCN2022088560-appb-000511
In certain embodiments, the deuterated compound is a compound structure (eg, L, eg, Ring A, Ring B, L in LA, LA-1, LA-2, LA-3, LA-4, LA-5 3. A structure in which 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 Hs in ring C) are replaced by deuterium. In certain embodiments, the deuterated LA structure is
Figure PCTCN2022088560-appb-000510
Figure PCTCN2022088560-appb-000511
在某些实施方案中，所述氘代化物具有如下任一结构：In certain embodiments, the deuterated compound has any of the following structures:
Figure PCTCN2022088560-appb-000512
Figure PCTCN2022088560-appb-000512
Figure PCTCN2022088560-appb-000513
Figure PCTCN2022088560-appb-000513
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐的制备方法。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or The preparation method of its pharmaceutically acceptable salt.
本发明提供了一种药物组合物，包括治疗有效量的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，以及药学上可接受的载体、稀释剂或赋形剂。The present invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, and solvates , metabolites, prodrugs and/or pharmaceutically acceptable salts thereof, and pharmaceutically acceptable carriers, diluents or excipients.
本发明提供了一种降解SOS1蛋白的方法，包括使式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物与SOS1蛋白接触。The present invention provides a method for degrading SOS1 protein, comprising making the compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, The metabolite, prodrug and/or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof, is contacted with the SOS1 protein.
本发明提供了一种所述式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物用作治疗或预防SOS1介导的疾病或病症的药物使用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and /or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof for use as a medicament for treating or preventing SOS1-mediated diseases or disorders.
本发明提供了一种所述式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物用作治疗或预防由SOS1与Ras(例如KRAS)或者SOS1与Rac(例如KRAS)相互作用所引起的疾病或病症(癌症)的药物的应用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and /or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof for use as a medicament for the treatment or prevention of a disease or disorder (cancer) caused by the interaction of SOS1 with Ras (eg KRAS) or SOS1 and Rac (eg KRAS) application.
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物在制备治疗或预防SOS1介导的疾病或病症的药物(例如癌症)中的应用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or Use of a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof, in the manufacture of a medicament for the treatment or prevention of SOS1-mediated diseases or disorders (eg, cancer).
本发明提供了式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物在制备治疗或预防由SOS1与Ras(例如 KRAS)或者SOS1与Rac(例如KRAS)相互作用所引起的疾病或病症(例如癌症)的药物的应用。The present invention provides compounds of formula I, and/or stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or pharmaceuticals thereof Use of an acceptable salt of the above, or a pharmaceutical composition thereof, in the manufacture of a medicament for the treatment or prevention of a disease or disorder (eg, cancer) caused by the interaction of SOS1 and Ras (eg, KRAS) or SOS1 and Rac (eg, KRAS).
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物在制备治疗或预防癌症药物中的应用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or Use of a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof in the preparation of a medicament for treating or preventing cancer.
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物在制备治疗或预防胰腺癌、肺癌、结肠直肠癌、胆管上皮癌、多发性骨髓瘤、黑色素瘤、子宫癌、子宫内膜癌、甲状腺癌、急性髓性白血病、膀胱癌、尿路上皮癌、胃癌、子宫颈癌、头颈部鳞状细胞癌、弥漫性大B细胞淋巴瘤、食道癌、慢性淋巴细胞性白血病、肝细胞癌、乳腺癌、卵巢癌、前列腺癌、成胶质细胞瘤、肾癌及肉瘤药物的应用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or Its pharmaceutically acceptable salt, or its pharmaceutical composition is used in the preparation of treatment or prevention of pancreatic cancer, lung cancer, colorectal cancer, bile duct epithelial cancer, multiple myeloma, melanoma, uterine cancer, endometrial cancer, thyroid cancer, Acute myeloid leukemia, bladder cancer, urothelial cancer, gastric cancer, cervical cancer, head and neck squamous cell carcinoma, diffuse large B-cell lymphoma, esophageal cancer, chronic lymphocytic leukemia, hepatocellular carcinoma, breast cancer , ovarian cancer, prostate cancer, glioblastoma, renal cancer and sarcoma drug application.
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物在制备治疗或预防1型神经纤维瘤病(NF1)、努南综合征(NS)、伴有多雀斑的努南综合征(NSML)、毛细血管畸形-动静脉畸形综合征(CM-AVM)、科斯特洛综合征(CS)、心-面-皮肤综合症(CFC)、莱格斯综合征和遗传性牙龈纤维瘤病药物的应用。The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or A pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof in the preparation of the treatment or prevention of neurofibromatosis type 1 (NF1), Noonan syndrome (NS), Noonan syndrome with multiple freckles (NSML), capillary Vascular malformation-arteriovenous malformation syndrome (CM-AVM), Costello syndrome (CS), cardio-facial-cutaneous syndrome (CFC), Leggers syndrome and hereditary gingival fibromatosis.
本发明提供一种治疗或预防由SOS1介导的疾病或病症的方法，包括向有需要的患者施用治疗有效量的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物。The present invention provides a method of treating or preventing a disease or disorder mediated by SOS1, comprising administering to a patient in need thereof a therapeutically effective amount of a compound of formula I, and/or a stereoisomer, enantiomer, non- Enantiomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.
本发明提供一种治疗或预防由SOS1与Ras(例如KRAS)或者SOS1与Rac(例如KRAS)相互作用调控的疾病或病症(例如癌症)的方法，包括向有需要的患者施用治疗有效量的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物。The present invention provides a method of treating or preventing a disease or disorder (eg, cancer) modulated by the interaction of SOS1 and Ras (eg, KRAS) or SOS1 and Rac (eg, KRAS), comprising administering to a patient in need thereof a therapeutically effective amount of a formula Compound I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or pharmaceutically acceptable salts thereof , or its pharmaceutical composition.
本发明某些实施方案中，所述的癌症可选自：In certain embodiments of the present invention, the cancer may be selected from:
心脏:肉瘤(血管肉瘤、纤维肉瘤、横纹肌肉瘤、脂肪肉瘤)、黏液瘤、横纹肌瘤、纤维瘤、脂肪瘤和畸胎瘤组；Cardiac: Sarcomas (angiosarcoma, fibrosarcoma, rhabdomyosarcoma, liposarcoma), myxoma, rhabdomyomas, fibroids, lipomas and teratoma groups;
肺:支气管癌(鳞状细胞癌、未分化小细胞癌、未分化大细胞癌、腺癌)、肺泡癌(细支气管癌)、支气管腺瘤、肉瘤、淋巴瘤、软骨瘤错构瘤、间皮瘤；Lung: Bronchial carcinoma (squamous cell carcinoma, undifferentiated small cell carcinoma, undifferentiated large cell carcinoma, adenocarcinoma), alveolar carcinoma (bronchiolar carcinoma), bronchial adenoma, sarcoma, lymphoma, chondroma, hamartoma, interstitial carcinoma skin tumor;
胃肠道食管(鳞状细胞癌、腺癌、平滑肌肉瘤、淋巴瘤)、胃(癌、淋巴瘤、平滑肌肉瘤)、胰腺(导管腺癌、胰岛素瘤、胰高血糖素瘤、胃泌素瘤、类癌肿瘤、血管活性肠肽瘤)、小肠(腺癌、淋巴瘤、类癌肿瘤、卡波西氏肉瘤、平滑肌瘤、血管瘤、脂肪瘤、神经纤维瘤、纤维瘤)、大肠(腺癌、管状腺瘤、绒毛腺瘤、错构瘤、平滑肌瘤)；Gastrointestinal esophagus (squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma), stomach (cancer, lymphoma, leiomyosarcoma), pancreas (ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma , carcinoid tumor, vasoactive intestinal peptide tumor), small intestine (adenocarcinoma, lymphoma, carcinoid tumor, Kaposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, fibroma), large intestine ( adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, leiomyoma);
泌尿生殖系统:肾(腺癌、肾母细胞瘤、淋巴瘤、白血病)、膀胱和尿道(鳞状细胞癌、移行细胞癌、腺癌)、前列腺(腺癌、肉瘤)、睾丸(精原细胞瘤、畸胎瘤、胚胎癌、畸胎瘤、绒毛膜癌、肉瘤、间质细胞癌、纤维瘤、纤维腺瘤、腺瘤样瘤、脂肪瘤)；Genitourinary System: Kidney (adenocarcinoma, Wilms tumor, lymphoma, leukemia), bladder and urethra (squamous cell carcinoma, transitional cell carcinoma, adenocarcinoma), prostate (adenocarcinoma, sarcoma), testis (spermatogonia) tumor, teratoma, embryonal carcinoma, teratoma, choriocarcinoma, sarcoma, mesenchymal cell carcinoma, fibroma, fibroadenoma, adenomatous tumor, lipoma);
肝:肝癌(肝细胞癌)、胆管癌、肝母细胞瘤、血管肉瘤、肝细胞腺瘤、血管瘤；Liver: liver cancer (hepatocellular carcinoma), cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, hemangioma;
胆道:胆囊癌、壶腹癌、胆管癌；Biliary tract: gallbladder cancer, ampullary cancer, cholangiocarcinoma;
骨:骨肉瘤(骨肉瘤)、纤维肉瘤、恶性纤维组织细胞瘤、软骨肉瘤、尤因氏肉瘤、恶性淋巴瘤(网状细胞肉瘤)、多发性骨髓瘤、恶性巨细胞瘤脊索瘤、软骨瘤(骨软骨外生骨病)、良性软骨瘤、成软骨瘤、软骨黏液纤维瘤、骨样骨瘤和巨细胞瘤；Bone: Osteosarcoma (osteosarcoma), fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma, malignant giant cell tumor chordoma, chondroma (extrachondral bone disease), benign chondroma, chondroblastoma, chondromyxofibroma, osteoid osteoma, and giant cell tumor;
神经系统:颅骨(骨瘤、血管瘤、肉芽肿、黄色瘤、畸形骨炎)、脑膜(脑膜瘤、脑膜肉瘤、胶质瘤)、大脑(星形细胞瘤、髓母细胞瘤、胶质瘤、室管膜瘤、生发细胞瘤(松果体瘤)、多形胶质母细胞瘤、少突胶质母细胞瘤、神经鞘瘤、视网膜母细胞瘤、先天性肿瘤)、脊髓神经纤维瘤、脑膜瘤、胶质瘤、肉瘤)；Nervous system: skull (osteomas, hemangiomas, granulomas, xanthomas, osteitis malformations), meninges (meningiomas, meningiosarcomas, gliomas), brain (astrocytomas, medulloblastomas, gliomas) , ependymoma, germinoma (pineal tumor), glioblastoma multiforme, oligodendroglioma, schwannoma, retinoblastoma, congenital tumors), spinal neurofibromas , meningioma, glioma, sarcoma);
妇科:子宫(子宫内膜癌(浆液性囊腺癌、粘液性囊腺癌、未分类癌)、颗粒-鞘膜细胞瘤、支持间质细胞瘤、无生殖细胞瘤、恶性畸胎瘤)、外阴(鳞状细胞癌、上皮内癌、腺癌、纤维肉瘤、黑素瘤)、阴道(透明细胞癌、鳞状细胞癌、葡萄状肉瘤(胚胎型横纹肌肉瘤)、输卵管(癌)；Gynecology: Uterine (endometrial carcinoma (serous cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified carcinoma), granular-schingmocytoma, Sertoli stromal cell tumor, germ cell tumor, malignant teratoma), Vulva (squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, melanoma), vagina (clear cell carcinoma, squamous cell carcinoma, grape sarcoma (embryonic rhabdomyosarcoma), fallopian tube (cancer);
血液学:血液(髓系白血病(急性和慢性)、急性淋巴母细胞白血病、慢性淋巴细胞白血病、骨髓增生性疾病、多发性骨髓瘤、骨髓增生异常综合征)、霍奇金病、非霍奇金淋巴瘤(恶性淋巴瘤)；Hematology: Hematology (myeloid leukemia (acute and chronic), acute lymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferative disorders, multiple myeloma, myelodysplastic syndromes), Hodgkin's disease, non-Hodgkin's Gold lymphoma (malignant lymphoma);
皮肤:恶性黑色素瘤、基底细胞癌、鳞状细胞癌、卡波西肉瘤、痣发育不良痣、脂肪瘤、血管瘤、皮肤纤维瘤、瘢痕疙瘩、银屑病；Skin: malignant melanoma, basal cell carcinoma, squamous cell carcinoma, Kaposi's sarcoma, nevus dysplasia, lipoma, hemangioma, dermatofibroma, keloid, psoriasis;
肾上腺:成神经细胞瘤。Adrenal gland: neuroblastoma.
本发明某些实施方案中，所述的癌症可选自胰腺癌、肺癌、结肠直肠癌、胆管上皮癌、多发性骨髓瘤、黑色素瘤、子宫癌、子宫内膜癌、甲状腺癌、急性髓性白血病、膀胱癌、尿路上皮癌、胃癌、子宫颈癌、头颈部鳞状细胞癌、弥漫性大B细胞淋巴瘤、食道癌、慢性淋巴细胞性白血病、肝细胞癌、乳腺癌、卵巢癌、前列腺癌、成胶质细胞瘤、肾癌及肉瘤。In certain embodiments of the present invention, the cancer can be selected from pancreatic cancer, lung cancer, colorectal cancer, bile duct epithelial cancer, multiple myeloma, melanoma, uterine cancer, endometrial cancer, thyroid cancer, acute myeloid cancer Leukemia, bladder cancer, urothelial cancer, gastric cancer, cervical cancer, head and neck squamous cell carcinoma, diffuse large B-cell lymphoma, esophageal cancer, chronic lymphocytic leukemia, hepatocellular carcinoma, breast cancer, ovarian cancer , prostate cancer, glioblastoma, kidney cancer and sarcoma.
本发明还提供了一种前述的式Ⅰ化合物，和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐或前述的药物组合物在制备用于治疗和/或预防KRAS介导的疾病或病症的药物中的应用。The present invention also provides a aforementioned compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or Use of a pharmaceutically acceptable salt thereof or the aforementioned pharmaceutical composition in the preparation of a medicament for the treatment and/or prevention of KRAS-mediated diseases or disorders.
本发明还提供了一种治疗和/或预防KRAS介导的疾病或病症的方法，包括向有需要的患者施用治疗有效量的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐，或其药物组合物。The present invention also provides a method of treating and/or preventing a KRAS-mediated disease or disorder, comprising administering to a patient in need thereof a therapeutically effective amount of a compound of formula I, and/or a stereoisomer, enantiomer thereof isomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.
本发明某些实施方案中，所述的KRAS可为突变型KRAS。所述突变型KRAS优选为KRAS G12C、KRAS G12D、KRAS G13D和KRAS G12V中的一种或多种。In certain embodiments of the present invention, the KRAS may be a mutant KRAS. The mutant KRAS is preferably one or more of KRAS G12C, KRAS G12D, KRAS G13D and KRAS G12V.
本发明提供了一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐的制备方法：The present invention provides a compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or The preparation method of its pharmaceutically acceptable salt:
当S为S6c
Figure PCTCN2022088560-appb-000514
L为LA
Figure PCTCN2022088560-appb-000515
且环B含有NH基团时，制备方法为： When S is S6c
Figure PCTCN2022088560-appb-000514
L is LA
Figure PCTCN2022088560-appb-000515
And when ring B contains an NH group, the preparation method is:
Figure PCTCN2022088560-appb-000516
Figure PCTCN2022088560-appb-000516
INT-A与INT-B发生还原胺化反应得到目标化合物；其中所述还原胺化的还原试剂包括但不限于Pd/C、硼氢化钠、氰基硼氢化钠、硼烷、三乙酰氧基硼氢化钠。其中所述
Figure PCTCN2022088560-appb-000517
指含有NH基团的环B；R 2、R 3、 R 4、R 5、R 6、R 7如S6b中所定义和描述；
Figure PCTCN2022088560-appb-000518
指含有醛基的L 3；、环A、环B、环C、X”如LA中所定义；E如本发明中所定义和描述，优选E为E7、E7a、E7b、E7c、E7d、E7e、E7a-1、E7a-2、E21、E21-1a、E21-1b、E21-1c、E21-1d、E21-1e、E21-1f、E21-1g、E21-1h、E21-1aa、E21-1bb、E21-1cc、E21-1dd、E21-1ee、E21-1ff、E21-1gg或E21-1hh。 INT-A and INT-B undergo reductive amination reaction to obtain the target compound; wherein the reducing reagents for the reductive amination include but are not limited to Pd/C, sodium borohydride, sodium cyanoborohydride, borane, triacetoxy Sodium borohydride. wherein the
Figure PCTCN2022088560-appb-000517
refers to Ring B containing an NH group; R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6b;
Figure PCTCN2022088560-appb-000518
refers to L 3 containing an aldehyde group; Ring A, Ring B, Ring C, X" are as defined in LA; E is as defined and described in the present invention, preferably E is E7, E7a, E7b, E7c, E7d, E7e , E7a-1, E7a-2, E21, E21-1a, E21-1b, E21-1c, E21-1d, E21-1e, E21-1f, E21-1g, E21-1h, E21-1aa, E21-1bb , E21-1cc, E21-1dd, E21-1ee, E21-1ff, E21-1gg or E21-1hh.
当S为S6c
Figure PCTCN2022088560-appb-000519
L为LA
Figure PCTCN2022088560-appb-000520
且环C含有NH基团，X”为C(O)时，制备方法为： When S is S6c
Figure PCTCN2022088560-appb-000519
L is LA
Figure PCTCN2022088560-appb-000520
And ring C contains NH group, when X" is C(O), the preparation method is:
Figure PCTCN2022088560-appb-000521
Figure PCTCN2022088560-appb-000521
INT-C与INT-D碱性条件下发生取代反应得到目标化合物；其中所述碱包括但不限于三乙胺、N,N-二异丙基乙胺、碳酸钾、碳酸钠、碳酸氢钠。其中
Figure PCTCN2022088560-appb-000522
指含有NH基团的环C；P 100为五氟苯基或者对硝基苯基；R 2、R 3、R 4、R 5、R 6、R 7如S6b中所定义和描述；环A、环B、环C、L 3如LA中所定义；E如本发明中所定义和描述，优选E为E7、E7a、E7b、E7c、E7d、E7e、E7a-1、E7a-2、E21、E21-1a、E21-1b、E21-1c、E21-1d、E21-1e、E21-1f、E21-1g、E21-1h、E21-1aa、E21-1bb、E21-1cc、E21-1dd、E21-1ee、E21-1ff、E21-1gg或E21-1hh。 Substitution reaction occurs between INT-C and INT-D under alkaline conditions to obtain the target compound; wherein the base includes but not limited to triethylamine, N,N-diisopropylethylamine, potassium carbonate, sodium carbonate, sodium bicarbonate . in
Figure PCTCN2022088560-appb-000522
Refers to ring C containing an NH group; P 100 is pentafluorophenyl or p-nitrophenyl; R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6b; ring A , Ring B, Ring C, L 3 are as defined in LA; E is as defined and described in the present invention, preferably E is E7, E7a, E7b, E7c, E7d, E7e, E7a-1, E7a-2, E21, E21-1a, E21-1b, E21-1c, E21-1d, E21-1e, E21-1f, E21-1g, E21-1h, E21-1aa, E21-1bb, E21-1cc, E21-1dd, E21- 1ee, E21-1ff, E21-1gg or E21-1hh.
当S为S6d
Figure PCTCN2022088560-appb-000523
L为LA
Figure PCTCN2022088560-appb-000524
且环C含有NH基团，X”为C(O)时，制备方法为： When S is S6d
Figure PCTCN2022088560-appb-000523
L is LA
Figure PCTCN2022088560-appb-000524
And ring C contains NH group, when X" is C(O), the preparation method is:
Figure PCTCN2022088560-appb-000525
Figure PCTCN2022088560-appb-000525
INT-E与INT-D碱性条件下发生取代反应得到目标化合物；其中所述碱包括但不限于三乙胺、N,N-二异丙基乙胺、碳酸钾、碳酸钠、碳酸氢钠。其中
Figure PCTCN2022088560-appb-000526
指含有NH基团的环C；P 100为五氟苯基或者对硝基苯基；R 2、R 3、R 4、R 5、R 6、R 7如S6d中所定义和描述；环A、环B、环C、L 3如LA中所定义；E如本发明中所定义和描述，优选E为E7、E7a、E7b、E7c、E7d、E7e、E7a-1、E7a-2、E21、E21-1a、E21-1b、E21-1c、E21-1d、E21-1e、E21-1f、E21-1g、E21-1h、E21-1aa、E21-1bb、E21-1cc、E21-1dd、E21-1ee、E21-1ff、E21-1gg或E21-1hh、。 Substitution reaction occurs between INT-E and INT-D under alkaline conditions to obtain the target compound; wherein the base includes but is not limited to triethylamine, N,N-diisopropylethylamine, potassium carbonate, sodium carbonate, sodium bicarbonate . in
Figure PCTCN2022088560-appb-000526
refers to ring C containing an NH group; P 100 is pentafluorophenyl or p-nitrophenyl; R 2 , R 3 , R 4 , R 5 , R 6 , R 7 are as defined and described in S6d; ring A , Ring B, Ring C, L 3 are as defined in LA; E is as defined and described in the present invention, preferably E is E7, E7a, E7b, E7c, E7d, E7e, E7a-1, E7a-2, E21, E21-1a, E21-1b, E21-1c, E21-1d, E21-1e, E21-1f, E21-1g, E21-1h, E21-1aa, E21-1bb, E21-1cc, E21-1dd, E21- 1ee, E21-1ff, E21-1gg or E21-1hh,.
详细说明：除非有相反陈述、下列用在说明书和权利要求书中的术语具有下述含义。DETAILED DESCRIPTION: Unless stated to the contrary, the following terms used in the specification and claims have the following meanings.
“烷基”是指饱和的脂肪族烃基团，包括直链或支链烷基；C 1-C 8烷基是指含有1-8个碳原子的烷基，例如甲基、乙基、正丙基、异丙基、正丁基、异丁基、叔丁基、仲丁基、正戊基、1、1-二甲基丙基、1、2-二甲基丙基、2、2-二甲基丙基、1-乙基丙基、2-甲基丁基、3-甲基丁基、正己基、1-乙基-2-甲基丙基、1、1、2-三甲基丙基、1、1-二甲基丁基、1、2-二甲基丁基、2、2-二甲基丁基、1、3-二甲基丁基、2-乙基丁基、2-甲基戊基、3-甲基戊基、4-甲基戊基、2、3-二甲基丁基、正庚基、2-甲基己基、3-甲基己基、4-甲基己基、5-甲基己基、2、3-二甲基戊基、2、4-二甲基戊基、2、2-二甲基戊基、3、3-二甲基戊基、2-乙基戊基、3-乙基戊基、正辛基、2、3-二甲基己基、2、4-二甲基己基、2、5-二甲基己基、2、2-二甲基己基、3、3-二甲基己基、4、4-二甲基己基、2-乙基己基、3-乙基己基、4-乙基己基、2-甲基-2-乙基戊基、2-甲基-3-乙基戊基或其各种支链异构体；优选C 1-C 6烷基；更优选C 1-C 4烷基。所述烷基可以是取代的或未取代的。在一些实施方案中，所述烷基为C 1、C 2、C 3、C 4、C 5、C 6、C 7或C 8烷基。 "Alkyl" refers to saturated aliphatic hydrocarbon groups, including straight or branched chain alkyl groups; C 1 -C 8 alkyl groups refer to alkyl groups containing 1-8 carbon atoms, such as methyl, ethyl, n- Propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, n-pentyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2, 2 - Dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-tri Methylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl , 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl, n-heptyl, 2-methylhexyl, 3-methylhexyl, 4 -Methylhexyl, 5-methylhexyl, 2,3-dimethylpentyl, 2,4-dimethylpentyl, 2,2-dimethylpentyl, 3,3-dimethylpentyl , 2-ethylpentyl, 3-ethylpentyl, n-octyl, 2,3-dimethylhexyl, 2,4-dimethylhexyl, 2,5-dimethylhexyl, 2,2- Dimethylhexyl, 3,3-dimethylhexyl, 4,4-dimethylhexyl, 2-ethylhexyl, 3-ethylhexyl, 4-ethylhexyl, 2-methyl-2-ethyl Pentyl, 2-methyl-3-ethylpentyl or various branched chain isomers thereof; preferably C1 - C6 alkyl; more preferably C1 - C4 alkyl. The alkyl group may be substituted or unsubstituted. In some embodiments, the alkyl group is a C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 7 , or C 8 alkyl.
“环烷基”指饱和或部分不饱和的单环或多环环状烃取代基；“C 3-C 11环烷基”指包括3至11个碳原子的环烷基；“C 3-C 8元环烷基”指包括3至8个碳原子的环烷基；“C 5-C 10元环烷基”指包括5至10个碳原子的 环烷基； "Cycloalkyl" refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent; "C 3 -C 11 cycloalkyl" refers to a cycloalkyl group comprising 3 to 11 carbon atoms; "C 3 -C 11 cycloalkyl""C 8 -membered cycloalkyl" refers to a cycloalkyl group including 3 to 8 carbon atoms; "C 5 -C 10 -membered cycloalkyl" refers to a cycloalkyl group including 5 to 10 carbon atoms;
单环环烷基的非限制性实施例包含环丙基、环丁基、环戊基、环戊烯基、环己基、环己烯基、环己二烯基、环庚基、环庚三烯基、环辛基等，优选环丙基、环丁基、环戊基、环己基；优选C 3-C 8元环烷基；更优选C 3-C 6元环烷基。 Non-limiting examples of monocyclic cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cyclohexadienyl, cycloheptyl, cycloheptyl Alkenyl, cyclooctyl, etc., preferably cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl; preferably C3 - C8 -membered cycloalkyl; more preferably C3 - C6 -membered cycloalkyl.
多环环烷基包括螺环、稠环和桥环的环烷基。“螺环烷基”指单环之间共用一个碳原子(称螺原子)的多环基团，他们可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统。根据环与环之间共用螺原子的数目将螺环烷基分为单螺环烷基、双螺环烷基基或多螺环烷基，优选7-12元双螺环烷基。螺环烷基的非限制性实施例包含：Polycyclic cycloalkyl groups include spiro, fused and bridged cycloalkyl groups. "Spirocycloalkyl" refers to a polycyclic group in which a single carbon atom (called a spiro atom) is shared between the single rings. They may contain one or more double bonds, but none of the rings have a fully conjugated pi electron system. According to the number of spiro atoms shared between the rings, spirocycloalkyl groups are classified into mono-spirocycloalkyl groups, double-spirocycloalkyl groups or poly-spirocycloalkyl groups, preferably 7-12 membered double-spirocycloalkyl groups. Non-limiting examples of spirocycloalkyl include:
Figure PCTCN2022088560-appb-000527
Figure PCTCN2022088560-appb-000527
“稠环烷基”指系统中的每个环与体系中的其他环共享毗邻的一对碳原子的全碳多环基团，其中一个或多个环可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统。根据组成环的数目可以分为双环、三环、四环或多环稠环烷基，优选双环稠环烷基。稠环烷基的非限制性实施例包含："Fused cycloalkyl" refers to an all-carbon polycyclic group in which each ring in the system shares an adjacent pair of carbon atoms with other rings in the system, wherein one or more rings may contain one or more double bonds, but None of the rings have a fully conjugated pi electron system. According to the number of constituent rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic fused cycloalkyl, preferably bicyclic fused cycloalkyl. Non-limiting examples of fused cycloalkyl groups include:
Figure PCTCN2022088560-appb-000528
Figure PCTCN2022088560-appb-000528
“桥环烷基”指任意两个环共用两个不直接连接的碳原子的全碳多环基团，他们可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统，根据组成环的数目可以分为双环、三环、四环或多环桥环烷基。桥环烷基的非限制性实施例包含："Bridged cycloalkyl" refers to an all-carbon polycyclic group in which any two rings share two non-directly connected carbon atoms, they may contain one or more double bonds, but none of the rings have a fully conjugated pi-electron system , according to the number of rings can be divided into bicyclic, tricyclic, tetracyclic or polycyclic bridged cycloalkyl. Non-limiting examples of bridged cycloalkyl groups include:
Figure PCTCN2022088560-appb-000529
Figure PCTCN2022088560-appb-000529
所述环烷基环可以稠合于芳基、杂芳基或杂环烷基环上，其中与母体结构连接在一起的环为环烷基，非限制性实施例包括茚满基、四氢萘基、苯并环庚烷基等。所述环烷基可以是任选取代的或未取代的。The cycloalkyl ring can be fused to an aryl, heteroaryl or heterocycloalkyl ring, wherein the ring connected to the parent structure is a cycloalkyl, non-limiting examples include indanyl, tetrahydro Naphthyl, benzocycloheptyl, etc. The cycloalkyl group may be optionally substituted or unsubstituted.
在一些实施方案中，所述环烷基为C 3、C 4、C 5、C 6、C 7、C 8、C 9、C 10、C 11、C 12单环或多环(例如螺环、稠环或桥环)环烷基。 In some embodiments, the cycloalkyl is C 3 , C 4 , C 5 , C 6 , C 7 , C 8 , C 9 , C 10 , C 11 , C 12 monocyclic or polycyclic (eg, spirocyclic , fused ring or bridged ring) cycloalkyl.
“杂环烷基”指饱和的或部分不饱和的单环或多环环状烃取代基，其中一个或多个(例如2、3、4或5)环原子选自氮、氧或S(O) r(其中r是整数0、1或2)，但不包含-O-O-、-O-S-或-S-S-的环部分，其余环原子为碳。“3-11元杂环烷基”指包含3至11个环原子的环基，“5-10元杂环烷基”指包含5至10个环原子的环基，“3-8元杂环烷基”指包含3至8个环原子的环基，优选含有1-2个选自N、O或S杂原子的“3-11元杂环烷基”，更优选含有1个或2个N原子的3-11元杂环烷基。 "Heterocycloalkyl" refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent wherein one or more (eg 2, 3, 4 or 5) ring atoms are selected from nitrogen, oxygen or S ( O) r (wherein r is the integer 0, 1 or 2), but does not contain ring moieties of -OO-, -OS- or -SS- and the remaining ring atoms are carbons. "3-11 membered heterocycloalkyl" refers to a ring group containing 3 to 11 ring atoms, "5-10 membered heterocycloalkyl" refers to a ring group containing 5 to 10 ring atoms, "3-8 membered heterocycloalkyl""Cycloalkyl" refers to a ring group containing 3 to 8 ring atoms, preferably "3-11 membered heterocycloalkyl" containing 1-2 heteroatoms selected from N, O or S, more preferably containing 1 or 2 3- to 11-membered heterocycloalkyl with N atoms.
单环杂环烷基优选为含有1-2个N杂原子的3-8元单环杂环烷基；单环杂环烷基的非限制性实施例包含吡咯烷基、哌啶基、哌嗪基、吗啉基、硫代吗啉基、高哌嗪基等，优选哌啶基和哌嗪基。Monocyclic heterocycloalkyl is preferably a 3-8 membered monocyclic heterocycloalkyl containing 1-2 N heteroatoms; non-limiting examples of monocyclic heterocycloalkyl include pyrrolidinyl, piperidinyl, piperidine oxazinyl, morpholinyl, thiomorpholinyl, homopiperazinyl, etc., preferably piperidinyl and piperazinyl.
多环杂环烷基包括螺环、稠环和桥环的杂环烷基。“螺杂环烷基”指单环之间共用一个原子(称螺原子)的多环杂环烷基团，其中一个或多个环原子选自氮、氧或S(O) r(其中r是整数0、1、2)，其余环原子为碳。他们可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统。根据环与环之间共用螺原子的数目将螺环烷基分为单螺杂环烷基、双螺杂环烷基或多螺杂环烷基，优选含有1-2个选自N、O或S杂原子的饱和的“3-11元双螺杂环烷基”；更优选含有1个或2个N原子的饱和的“7-11元双螺杂环烷基”。螺杂环烷基的非限制性实施例包含： Polycyclic heterocycloalkyl groups include spiro, fused and bridged ring heterocycloalkyl groups. "Spiroheterocycloalkyl" refers to a polycyclic heterocycloalkyl group in which a single atom (called a spiro atom) is shared between the monocyclic rings, wherein one or more ring atoms are selected from nitrogen, oxygen, or S(O) r (where r are integers 0, 1, 2) and the remaining ring atoms are carbon. They can contain one or more double bonds, but none of the rings have a fully conjugated pi electron system. According to the number of spiro atoms shared between the rings, the spirocycloalkyl group is divided into single spiroheterocycloalkyl, double spiroheterocycloalkyl or polyspiroheterocycloalkyl, preferably containing 1-2 atoms selected from N, O or a saturated "3-11-membered bis-spiroheterocycloalkyl" of an S heteroatom; more preferably a saturated "7-11-membered bis-spiroheterocycloalkyl" containing 1 or 2 N atoms. Non-limiting examples of spiroheterocycloalkyl include:
Figure PCTCN2022088560-appb-000530
Figure PCTCN2022088560-appb-000530
“稠杂环烷基”指系统中的每个环与体系中的其他环共享毗邻的一对原子的多环杂环烷基团，一个或多个环可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统，其中一个或多个环原子选自氮、氧或S(O) r(其中r是整数0、1、2)，其余环原子为碳。根据组成环的数目可以分为双环、三环、四环或多环稠杂环烷基，优选含有1-3个选自N、O或S杂原子的“3-11元双环稠杂环烷基”；更优选含有1个或2个N原子的饱和的“3-11元双环稠杂环烷基”。稠杂环烷基的非限制性实施例包含： "Fused heterocycloalkyl" refers to a polycyclic heterocycloalkyl group in which each ring in the system shares an adjacent pair of atoms with other rings in the system, one or more rings may contain one or more double bonds, but None of the rings have a fully conjugated pi-electron system, where one or more ring atoms are selected from nitrogen, oxygen, or S(O) r (where r is an integer 0, 1, 2) and the remaining ring atoms are carbon. According to the number of rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic fused heterocycloalkanes, preferably "3-11-membered bicyclic fused heterocycloalkanes containing 1-3 heteroatoms selected from N, O or S"group"; more preferably a saturated "3-11 membered bicyclic fused heterocycloalkyl" containing 1 or 2 N atoms. Non-limiting examples of fused heterocycloalkyl include:
Figure PCTCN2022088560-appb-000531
Figure PCTCN2022088560-appb-000531
“桥杂环烷基”指任意两个环共用两个不直接连接的原子的多环杂环烷基团，他们可以含有一个或多个双键，但没有一个环具有完全共轭的π电子系统，其中一个或多个环原子选自氮、氧或S(O) r(其中r是整数0、1、2)，其余环原子为碳。根据组成环的数目可以分为双环、三环、四环或多环桥环烷基，桥杂环烷基的非限制性实施例包含： "Bridged heterocycloalkyl" refers to polycyclic heterocycloalkyl groups in which any two rings share two atoms that are not directly connected, they may contain one or more double bonds, but none of the rings have fully conjugated pi electrons System wherein one or more ring atoms are selected from nitrogen, oxygen or S(O) r (where r is an integer 0, 1, 2) and the remaining ring atoms are carbon. Bridged cycloalkyl groups can be classified as bicyclic, tricyclic, tetracyclic or polycyclic according to the number of constituent rings, non-limiting examples of bridged heterocycloalkyl include:
Figure PCTCN2022088560-appb-000532
Figure PCTCN2022088560-appb-000532
所述杂环烷基环可以稠合于芳基、杂芳基或环烷基环上，其中与母体结构连接在一起的环为杂环烷基，非限制性实施例包含：The heterocycloalkyl ring can be fused to an aryl, heteroaryl or cycloalkyl ring, wherein the ring linked to the parent structure is a heterocycloalkyl, non-limiting examples include:
Figure PCTCN2022088560-appb-000533
所述杂环烷基可以是任选取代的或未取代的。
Figure PCTCN2022088560-appb-000533
The heterocycloalkyl group can be optionally substituted or unsubstituted.
在一些实施方案中，所述杂环烷基为3、4、5、6、7、8、9、10、11、12元单环或多环(例如螺环、稠环或桥环)杂环烷基，其中杂原子的个数可以为1、2、3、4或5个，每个杂原子独立地为氮、氧或S(O) r(其中r是整数0、1或2)。 In some embodiments, the heterocycloalkyl is a 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 membered monocyclic or polycyclic (eg spiro, fused or bridged) heterocyclic Cycloalkyl in which the number of heteroatoms may be 1, 2, 3, 4 or 5, each heteroatom being independently nitrogen, oxygen or S(O) r (where r is the integer 0, 1 or 2) .
“芳基”指全碳单环或稠合多环(也就是共享毗邻碳原子对的环)且具有共轭的π电子体系的多环基团，“6-10元芳基”指含有6-10个碳的全碳芳基，例如苯基和萘基；优选苯基。所述芳基环可以稠合于杂芳基、杂环烷基或环烷基环上，其中与母体结构连接在一起的环为芳基环，非限制性实施例包含："Aryl" refers to an all-carbon monocyclic or fused polycyclic group (that is, rings that share adjacent pairs of carbon atoms) and a polycyclic group with a conjugated pi-electron system, and "6-10 membered aryl" refers to a group containing 6 to 10 members. -10 carbon percarbon aryl groups such as phenyl and naphthyl; preferably phenyl. The aryl ring can be fused to a heteroaryl, heterocycloalkyl or cycloalkyl ring, wherein the ring connected to the parent structure is an aryl ring, non-limiting examples include:
Figure PCTCN2022088560-appb-000534
Figure PCTCN2022088560-appb-000535
所述芳基可以是任选取代的或未取代的。在一些实施方案中，所述芳基为6-10元芳基。
Figure PCTCN2022088560-appb-000534
Figure PCTCN2022088560-appb-000535
The aryl group can be optionally substituted or unsubstituted. In some embodiments, the aryl group is a 6-10 membered aryl group.
“杂芳基”指包含1至4个杂原子的杂芳族体系，所述杂原子包括氮、氧或S(O) r(其中r是整数0、1、2)，5-6元杂芳基指含有5-6个环原子的杂芳族体系，5-10元杂芳基指含有5-10个环原子的杂芳族体系，优选5-6元杂芳基；更优选含有1个或2个N原子的5-6元杂芳基；非限制实施例包括呋喃基、噻吩基、吡啶基、吡咯基、N-烷基吡咯基、嘧啶基、吡嗪基、吡唑、咪唑基、三唑基、四唑基等；优选吡啶基。所述杂芳基环可以稠合于芳基、杂环烷基或环烷基环上，其中与母体结构连接在一起的环为杂芳基环，非限制性实施例包含： "Heteroaryl" refers to a heteroaromatic system containing 1 to 4 heteroatoms including nitrogen, oxygen or S(O) r (where r is an integer 0, 1, 2), 5-6 membered heteroatoms Aryl refers to a heteroaromatic system containing 5-6 ring atoms, 5-10 membered heteroaryl refers to a heteroaromatic system containing 5-10 ring atoms, preferably a 5-6 membered heteroaryl; more preferably contains 1 5-6 membered heteroaryl with 1 or 2 N atoms; non-limiting examples include furyl, thienyl, pyridyl, pyrrolyl, N-alkylpyrrolyl, pyrimidinyl, pyrazinyl, pyrazole, imidazole pyridyl, triazolyl, tetrazolyl, etc.; preferably pyridyl. The heteroaryl ring can be fused to an aryl, heterocycloalkyl or cycloalkyl ring, wherein the ring linked to the parent structure is a heteroaryl ring, non-limiting examples include:
Figure PCTCN2022088560-appb-000536
Figure PCTCN2022088560-appb-000537
所述杂芳基可以是任选取代的或未取代的。在一些实施方案中，所述杂芳基为5、6、7、8、9、10元杂芳基，其中杂原子的个数可以为1、2、3、4或5个，每个杂原子独立地为氮、氧或S。
Figure PCTCN2022088560-appb-000536
Figure PCTCN2022088560-appb-000537
The heteroaryl group can be optionally substituted or unsubstituted. In some embodiments, the heteroaryl group is a 5, 6, 7, 8, 9, or 10 membered heteroaryl group, wherein the number of heteroatoms can be 1, 2, 3, 4 or 5, each heteroatom The atoms are independently nitrogen, oxygen or S.
“烯基”指由至少两个碳原子和至少一个碳-碳双键组成的如上述所定义的烷基，“C 2- 8烯基”指含有2-8个碳的直链或支链烯基，包括但不限于乙烯基、1-丙烯基、2-丙烯基、1-、2-或3丁烯基等，优选“C 2- 6烯基”，更优选“C 2- 4烯基”。所述烯基可以是取代的或未取代的。在一些实施方案中，所述烯基为C 2、C 3、C 4、C 5、C 6、C 7、C 8烯基。 "Alkenyl" refers to an alkyl group as defined above consisting of at least two carbon atoms and at least one carbon-carbon double bond, and " C2-8 alkenyl" refers to a straight or branched chain containing 2-8 carbons Alkenyl, including but not limited to vinyl, 1-propenyl, 2-propenyl, 1-, 2- or 3-butenyl, etc., preferably "C 2-6 alkenyl", more preferably "C 2-4 alkene " base". The alkenyl group may be substituted or unsubstituted. In some embodiments, the alkenyl group is C2 , C3, C4 , C5 , C6 , C7 , C8 alkenyl.
“炔基”指至少两个碳原子和至少一个碳-碳三键组成的如上所定义的烷基，“C 2- 8炔基”指含有2-8个碳的直链或支链炔基，包括但不限于乙炔基、1-丙炔基、2-丙炔基、1-、2-或3-丁炔基，优选“C 2- 6炔基”，更优选“C 2- 4炔基”。所述炔基可以是取代的或未取代的。在一些实施方案中，所述炔基为C 2、C 3、C 4、C 5、C 6、C 7、C 8炔基。 "Alkynyl" refers to an alkyl group as defined above consisting of at least two carbon atoms and at least one carbon-carbon triple bond, and " C2-8alkynyl " refers to a straight or branched chain alkynyl group containing 2-8 carbons , including but not limited to ethynyl, 1-propynyl, 2-propynyl, 1-, 2- or 3-butynyl, preferably "C 2-6 alkynyl", more preferably "C 2-4 alkynyl " base". The alkynyl group may be substituted or unsubstituted. In some embodiments, the alkynyl group is C2 , C3, C4 , C5 , C6 , C7 , C8 alkynyl.
“亚基”指二价基团，如亚烷基指二价烷基，亚烯基指二价烯基，亚炔基指二价炔基，亚环烷基指二价环烷基，亚杂环烷基指二价杂环烷基，亚芳基指二价芳基，亚杂芳基指二价杂芳基，所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基如上所定义，所述亚基可以是任选取代的或未取代的。"Subgroup" refers to a divalent group, such as alkylene refers to a divalent alkyl group, alkenylene refers to a divalent alkenyl group, alkynylene refers to a divalent alkynyl group, cycloalkylene refers to a divalent cycloalkyl group, and Heterocycloalkyl refers to divalent heterocycloalkyl, arylene refers to divalent aryl, heteroarylene refers to divalent heteroaryl, the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkane Radyl, aryl, heteroaryl are as defined above, and the subunits may be optionally substituted or unsubstituted.
“卤代烷基”指任选的被一个或多个氟、氯、溴或碘原子取代的烷基，其中所述烷基如上所定义，非限制性实施例包括二氟甲基、二氯甲基、二溴甲基、三氟甲基、三氯甲基、三溴甲基等。"Haloalkyl" refers to an alkyl group optionally substituted with one or more fluorine, chlorine, bromine or iodine atoms, wherein the alkyl group is as defined above, non-limiting examples include difluoromethyl, dichloromethyl , dibromomethyl, trifluoromethyl, trichloromethyl, tribromomethyl, etc.
“羟基烷基”指任选被一个或多个-OH取代的烷基，其中所述烷基如上所定义，非限制性实施例包括羟甲基、羟乙基、羟基丙基、羟基异丙基。"Hydroxyalkyl" refers to an alkyl group optionally substituted with one or more -OH, wherein the alkyl group is as defined above, non-limiting examples include hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxyisopropyl base.
“烷氧基”指-O-烷基，其中所述烷基如上所定义，非限制性实施例包括甲氧基、乙氧基、异丙氧基、叔丁氧基等。"Alkoxy" refers to -O-alkyl, wherein the alkyl group is as defined above, non-limiting examples include methoxy, ethoxy, isopropoxy, t-butoxy, and the like.
“环烷氧基”指-O-环烷基，其中所述环烷基如上所定义，非限制性实施例包括环丙烷氧基、环丁烷氧基、 环戊烷氧基、环己烷氧基等。"Cycloalkoxy" refers to -O-cycloalkyl, wherein the cycloalkyl is as defined above, non-limiting examples include cyclopropanoxy, cyclobutanoxy, cyclopentyloxy, cyclohexane Oxygen, etc.
“杂环烷氧基”指-O-杂环烷基，其中所述杂环烷基如上所定义，非限制性实施例包括氮杂环丁烷氧基、氮杂环戊烷氧基、哌啶基氧基、哌嗪基氧基、氧杂环戊基氧基、氧杂环己基氧基等。"Heterocycloalkoxy" refers to -O-heterocycloalkyl, wherein the heterocycloalkyl is as defined above, non-limiting examples include azetidinyloxy, azetidineoxy, piperidine Peridyloxy, piperazinyloxy, oxolaneoxy, oxhexyloxy, and the like.
“-C(O)C 1-C 3烷基”指-C(O)-CH 3、-C(O)-CH 2CH 3等。 "-C(O) C1 - C3 alkyl" refers to -C(O) -CH3 , -C (O) -CH2CH3 , and the like.
“氰基”指-CN。"Cyano" refers to -CN.
“羟基”指-OH。"Hydroxy" refers to -OH.
“磺酰基”指-S(O) 2-。 "Sulfonyl" refers to -S(O) 2- .
“羧基”或“羧酸”指-COOH。"Carboxyl" or "carboxylic acid" refers to -COOH.
“氧代”指＝O基团。"Oxo" refers to the =O group.
“卤素”指氟、氯、溴或碘。"Halogen" refers to fluorine, chlorine, bromine or iodine.
“Pd(PPh 3) 2Cl 2”指(二氯二(三苯基磷)合钯)。 "Pd( PPh3 ) 2Cl2 " refers to (dichlorobis(triphenylphosphonium)palladium).
“TEA”指三乙胺。"TEA" refers to triethylamine.
“EA或EtOAc”指乙酸乙酯。"EA or EtOAc" refers to ethyl acetate.
“THF”指四氢呋喃。"THF" refers to tetrahydrofuran.
“NaBH 4”指硼氢化钠。 " NaBH4 " refers to sodium borohydride.
“DCM”指二氯甲烷。"DCM" refers to dichloromethane.
“Tf 2O”指三氟甲基磺酸酐。 " Tf2O " refers to trifluoromethanesulfonic anhydride.
“(Bpin) 2”指双频哪醇联硼酸酯。 "(Bpin) 2 " refers to bipinacol biborate.
“Pd(dppf) 2Cl 2”指1,1'-双二苯基膦二茂铁二氯化钯。 "Pd(dppf) 2 Cl 2 " refers to 1,1'-bisdiphenylphosphinoferrocene palladium dichloride.
“KOAc”指醋酸钾。"KOAc" refers to potassium acetate.
“DMF”指N，N-二甲基甲酰胺。"DMF" refers to N,N-dimethylformamide.
“NBS”指N-溴代琥珀酰亚胺。"NBS" refers to N-bromosuccinimide.
“EtOH”指乙醇。"EtOH" refers to ethanol.
“MeOH”指甲醇。"MeOH" refers to methanol.
“Pd/C”指钯/碳。"Pd/C" refers to palladium/carbon.
“Pd(OH) 2/C”指氢氧化钯/碳。 "Pd(OH) 2 /C" refers to palladium hydroxide/carbon.
“DMSO”指二甲基亚砜。"DMSO" refers to dimethyl sulfoxide.
“HATU”指2-(7-氮杂苯并三氮唑)-N,N,N',N'-四甲基脲六氟磷酸酯。"HATU" refers to 2-(7-azabenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate.
“TFA”指三氟醋酸。"TFA" refers to trifluoroacetic acid.
“NMP”指N-甲基吡咯烷酮。"NMP" refers to N-methylpyrrolidone.
“IBX”指2-碘酰基苯甲酸。"IBX" refers to 2-iodoylbenzoic acid.
“DIEA”指N,N-二异丙基乙胺。"DIEA" refers to N,N-diisopropylethylamine.
“STAB”指三乙酰氧基硼氢化钠。"STAB" refers to sodium triacetoxyborohydride.
“T 3P”指2,4,6-三丙基-1,3,5,2,4,6-三氧三磷酸-2,4,6-三氧化物。 "T3P" refers to 2,4,6-tripropyl-1,3,5,2,4,6 - trioxytriphosphoric acid-2,4,6-trioxide.
“NaOH”指氢氧化钠。"NaOH" refers to sodium hydroxide.
“DMAP”指4-二甲氨基吡啶。"DMAP" refers to 4-dimethylaminopyridine.
“TPSCl”指2,4,6-三异丙基苯磺酰氯。"TPSCl" refers to 2,4,6-triisopropylbenzenesulfonyl chloride.
“DPBS”指杜氏磷酸缓冲液。"DPBS" refers to Dulbecco's Phosphate Buffered Saline.
“Dess-Martin”指戴斯-马丁试剂。"Dess-Martin" refers to Dess-Martin reagents.
“PBS”指磷酸缓冲盐溶液。"PBS" refers to phosphate buffered saline.
“SDS-PAGE”指十二烷基硫酸钠-聚丙烯酰胺凝胶电泳。"SDS-PAGE" refers to sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
“PVDF”指聚偏二氟乙烯。"PVDF" refers to polyvinylidene fluoride.
“PE”指石油醚。"PE" refers to petroleum ether.
“NaHCO 3”指碳酸氢钠。 " NaHCO3 " refers to sodium bicarbonate.
“Na 2SO 4”指硫酸钠。 " Na2SO4 " refers to sodium sulfate .
“NH 4Cl”指氯化铵。 " NH4Cl " refers to ammonium chloride.
“AcOH”指醋酸。"AcOH" refers to acetic acid.
“HCl”指盐酸。"HCl" refers to hydrochloric acid.
“DCC”指N,N'-二环己基碳二亚胺。"DCC" refers to N,N'-dicyclohexylcarbodiimide.
“Ti(OEt) 4”指钛酸四乙酯。 "Ti(OEt) 4 " refers to tetraethyl titanate.
“L-Selectride”指三异丁基硼氢化锂。"L-Selectride" refers to lithium triisobutylborohydride.
“BOP”指六氟磷酸苯并三唑-1-氧基三(二甲氨基)磷"BOP" means benzotriazol-1-oxytris(dimethylamino)phosphorus hexafluorophosphate
“DBU”指1,8-二氮杂环[5,4,0]十一烯-7"DBU" refers to 1,8-diazacyclo[5,4,0]undecene-7
“LiOH.H 2O”指一水合氢氧化锂 "LiOH.H 2 O" refers to lithium hydroxide monohydrate
“EDCI”指1-(3-二甲氨基丙基)-3-乙基碳二亚胺盐酸盐。"EDCI" refers to 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride.
“NIS”N-碘代丁二酰亚胺。"NIS" N-iodosuccinimide.
“Ac 2O”指乙酸酐。 " Ac2O " refers to acetic anhydride.
“HOAc”指乙酸。"HOAc" refers to acetic acid.
“Hantzsch-ester”指1,4-二氢-2,6-二甲基-3,5-吡啶二羧酸二乙酯."Hantzsch-ester" refers to diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate.
“DMA”指二甲基乙酰胺。"DMA" refers to dimethylacetamide.
“NiBr 2(dtbpy)”指4,4-二-叔丁基联吡啶二溴化镍. "NiBr 2 (dtbpy)" refers to 4,4-di-tert-butylbipyridine nickel dibromide.
“K 2CO 3”指碳酸钾。 " K2CO3 " refers to potassium carbonate.
“9-BBN”指9-硼双环[3.3.1]壬烷。"9-BBN" refers to 9-borabicyclo[3.3.1]nonane.
“MTBE”指甲基叔丁基醚。"MTBE" refers to methyl tert-butyl ether.
“LiOH”指氢氧化锂。"LiOH" refers to lithium hydroxide.
“DCE”指二氯乙烷。"DCE" refers to dichloroethane.
“NaBH 3CN”指氰基硼氢化钠。 " NaBH3CN " refers to sodium cyanoborohydride.
“CBr 4”指四溴化碳。 " CBr4 " refers to carbon tetrabromide.
“PPh 3”指三苯基膦。 " PPh3 " refers to triphenylphosphine.
“n-BuLi”指正丁基锂。"n-BuLi" refers to n-butyllithium.
“NaH”指钠氢。"NaH" refers to sodium hydrogen.
“i-PrOH”指异丙醇。"i-PrOH" refers to isopropanol.
“ACN”指乙腈。"ACN" refers to acetonitrile.
“NH 4HCO 3”指碳酸氢铵。 " NH4HCO3 " refers to ammonium bicarbonate .
“m-CPBA”指间氯过氧苯甲酸。"m-CPBA" refers to meta-chloroperoxybenzoic acid.
“KI”指碘化钾。"KI" refers to potassium iodide.
“IPA”指间苯二甲酸"IPA" means isophthalic acid
“N 2H 4-H 2O”指水合肼。 " N2H4 - H2O " refers to hydrazine hydrate.
“NMI”指N-甲基咪唑。"NMI" refers to N-methylimidazole.
“TCFH”指四甲基氯代脲六氟膦酸酯"TCFH" means tetramethylchlorourea hexafluorophosphonate
“Ruphos Pd G2”指氯(2-二环己基膦基-2',6'-二-异丙氧基-1,1'-联苯基)(2-氨基-1,1'-联苯-2-基)钯(II)。"Ruphos Pd G2" means chloro(2-dicyclohexylphosphino-2',6'-di-isopropoxy-1,1'-biphenyl)(2-amino-1,1'-biphenyl) -2-yl)palladium(II).
“K 3PO 4”指磷酸钾。 " K3PO4 " refers to potassium phosphate .
“(Boc) 2O”指二碳酸二叔丁酯。 "(Boc) 2 O" refers to di-tert-butyl dicarbonate.
“Prep-HPLC”指制备高效液相色谱。"Prep-HPLC" refers to preparative high performance liquid chromatography.
“sat.”指饱和溶液。"sat." refers to a saturated solution.
“aq”指水溶液。"aq" refers to an aqueous solution.
本文的化学结构中，作为连接键的“-”表示单键，“＝”表示双键(未限定构型的情况下，其可以为反式或顺式)。In the chemical structure herein, "-" as a linking bond represents a single bond, and "=" represents a double bond (it may be trans or cis when the configuration is not limited).
“任选”意味着随后所描述地事件或环境可以但不必发生，该说明包括该事件或环境发生或不发生地场合。例如，“任选被烷基取代的杂环烷基团”意味着烷基可以但不必须存在，该说明包括杂环烷基团被烷基取代的情形和杂环烷基团不被烷基取代的情形。"Optional" means that the subsequently described event or circumstance can but need not occur, and that the description includes instances where the event or circumstance occurs or instances where it does not occur. For example, "a heterocycloalkyl group optionally substituted with an alkyl group" means that an alkyl group may, but need not, be present, and the specification includes the case where the heterocycloalkyl group is substituted with an alkyl group and the case where the heterocycloalkyl group is not substituted with an alkyl group replaced situation.
“取代的”指基团中的一个或多个氢原子、优选为最多5个、更优选为1～3个氢原子彼此独立地被相 应数目的取代基取代。不言而喻、取代基仅处在它们的可能的化学位置、本领域技术人员能够在不付出过多努力的情况下确定(通过实验或理论)可能或不可能的取代。例如具有游离氢的氨基或羟基与具有不饱和(如烯属)键的碳原子结合时可能是不稳定的。"Substituted" means that one or more hydrogen atoms, preferably up to 5, more preferably 1 to 3 hydrogen atoms in a group are independently of each other substituted with a corresponding number of substituents. It goes without saying that the substituents are only in their possible chemical positions, and the person skilled in the art can determine (either experimentally or theoretically) possible or impossible substitutions without undue effort. For example, amino or hydroxyl groups with free hydrogen may be unstable when combined with carbon atoms with unsaturated (eg, olefinic) bonds.
除非另有说明，本文所用术语“任选取代的”可以是未取代的或者取代的；当被取代时，取代基可以是一个或多个(例如2、3、4、5或6个)独立选自烷基、烯基、炔基、羟基、羟基烷基、卤代烷基、烷氧基、氨基、氨基烷基、氰基、卤素、氧代、环烷基、杂环烷基、芳基和杂芳基，所述烷基、烯基、炔基、羟基、羟基烷基、卤代烷基、烷氧基、氨基、氨基烷基任选被一个或多个(例如2、3、4、5或6个)环烷基、杂环烷基、芳基和杂芳基取代；所述环烷基、杂环烷基、芳基和杂芳基任选被一个或多个选自烷基、烯基、炔基、羟基、羟基烷基、卤代烷基、烷氧基、氨基、氨基烷基、氰基、卤素、氧代的基团取代。Unless otherwise specified, the term "optionally substituted" as used herein can be unsubstituted or substituted; when substituted, the substituents can be one or more (eg 2, 3, 4, 5 or 6) independently selected from the group consisting of alkyl, alkenyl, alkynyl, hydroxy, hydroxyalkyl, haloalkyl, alkoxy, amino, aminoalkyl, cyano, halogen, oxo, cycloalkyl, heterocycloalkyl, aryl and Heteroaryl, the alkyl, alkenyl, alkynyl, hydroxy, hydroxyalkyl, haloalkyl, alkoxy, amino, aminoalkyl optionally substituted by one or more (eg 2, 3, 4, 5 or 6) cycloalkyl, heterocycloalkyl, aryl and heteroaryl substituted; the cycloalkyl, heterocycloalkyl, aryl and heteroaryl are optionally substituted by one or more selected from alkyl, alkene radical, alkynyl, hydroxy, hydroxyalkyl, haloalkyl, alkoxy, amino, aminoalkyl, cyano, halogen, oxo group substitution.
“药物组合物”表示含有一种或多种本文所述化合物或其生理学上/可药用的盐或前体药物与其他化学组分的混合物、以及其他组分例如生理学/可药用的载体和赋形剂。药物组合物的目的是促进对生物体的给药、利于活性成分的吸收进而发挥生物活性。"Pharmaceutical composition" means a mixture containing one or more of the compounds described herein, or a physiologically/pharmaceutically acceptable salt or prodrug thereof, with other chemical components, and other components such as a physiological/pharmaceutically acceptable carrier and excipients. The purpose of the pharmaceutical composition is to facilitate the administration to the organism, facilitate the absorption of the active ingredient and then exert the biological activity.
本发明还提供式(I)化合物药学上可接受的盐。术语“药学上可接受的盐”是指相对无毒的本发明化合物的酸加成盐或碱加成盐。所述酸加成盐为本发明式(I)化合物与合适的无机酸或者有机酸形成的盐，这些盐可在化合物最后的分离和提纯过程中制备，或者可用纯化的式(I)化合物以其游离碱形式与适宜的有机酸或无机酸进行反应来制备。代表性酸加成盐包括氢溴酸盐、硫酸盐、硫酸氢盐、亚硫酸盐、乙酸盐、草酸盐、戊酸盐、油酸盐、棕榈酸盐、硬脂酸盐、月硅酸盐、硼酸盐、苯甲酸盐、乳酸盐、磷酸盐、磷酸氢盐、碳酸盐、碳酸氢盐、甲苯甲酸盐、柠檬酸盐、马来酸盐、富马酸盐、琥珀酸盐、苯甲酸盐、甲磺酸盐、对甲苯磺酸盐、葡萄糖酸盐、乳糖酸盐和月桂基磺酸盐等。所述碱加成盐为式(I)化合物与合适的无机碱或者有机碱形成的盐，包括例如与碱金属、碱土金属、季铵阳离子形成的盐，例如钠盐、锂盐、钾盐、钙盐、镁盐、四甲基季铵盐、四乙基季铵盐等；胺盐包括与氨(NH 3)、伯胺、仲胺或叔胺形成的盐，如甲胺盐、二甲胺盐、三甲胺盐、三乙胺盐、乙胺盐等。 The present invention also provides pharmaceutically acceptable salts of the compounds of formula (I). The term "pharmaceutically acceptable salts" refers to relatively nontoxic acid or base addition salts of compounds of the present invention. The acid addition salts are salts of the compounds of formula (I) of the present invention with suitable inorganic or organic acids. These salts can be prepared during the final isolation and purification of the compounds, or the purified compounds of formula (I) can be used as It is prepared by reacting its free base form with a suitable organic or inorganic acid. Representative acid addition salts include hydrobromide, sulfate, bisulfate, sulfite, acetate, oxalate, valerate, oleate, palmitate, stearate, lauronate acid salt, borate, benzoate, lactate, phosphate, hydrogen phosphate, carbonate, bicarbonate, toluate, citrate, maleate, fumarate, Succinate, benzoate, mesylate, p-toluenesulfonate, gluconate, lactobionate, lauryl sulfonate, etc. The base addition salts are salts of compounds of formula (I) with suitable inorganic or organic bases, including, for example, salts with alkali metals, alkaline earth metals, quaternary ammonium cations, such as sodium salts, lithium salts, potassium salts, Calcium salts, magnesium salts, tetramethyl quaternary ammonium salts, tetraethyl quaternary ammonium salts, etc.; amine salts include salts with ammonia (NH 3 ), primary, secondary or tertiary amines, such as methylamine salts, dimethylamine Amine salt, trimethylamine salt, triethylamine salt, ethylamine salt, etc.
本发明的化合物或其药学上可接受的盐可给药于哺乳动物包括人，可口服、直肠、肠胃外(静脉内、肌肉内或皮下)、局部给药(粉剂、软膏剂或滴剂)、或瘤内给药。The compounds of the present invention, or pharmaceutically acceptable salts thereof, can be administered to mammals, including humans, orally, rectally, parenterally (intravenously, intramuscularly or subcutaneously), topically (in powders, ointments or drops) , or intratumoral administration.
本发明化合物的给药剂量可以大约为0.05-300mg/kg体重/天，优选10-300mg/kg体重/天，更优选10-200mg/kg体重/天。The compounds of the present invention may be administered at a dose of approximately 0.05-300 mg/kg body weight/day, preferably 10-300 mg/kg body weight/day, more preferably 10-200 mg/kg body weight/day.
本发明化合物或其药学上可接受的盐可以配制为用于口服给药的固体剂型，包括但不限于胶囊剂、片剂、丸剂、散剂和颗粒剂等。在这些固体剂型中，本发明式(I)化合物作为活性成分与至少一种常规惰性赋形剂(或载体)混合，例如与柠檬酸钠或磷酸二钙，或与下述成分混合：(1)填料或增容剂，如淀粉、乳糖、蔗糖、葡萄糖、甘露醇和硅酸等；(2)粘合剂，如羟甲基纤维素、藻酸盐、明胶、聚乙烯基吡咯烷酮、蔗糖和阿拉伯胶等；(3)保湿剂，如甘油等；(4)崩解剂，如琼脂、碳酸钙、马铃薯淀粉或木薯淀粉、藻酸、某些复合硅酸盐和碳酸钠等；(5)缓溶剂，如石蜡等；(6)吸收加速剂，如季铵化合物等；(7)润湿剂如鲸蜡醇和单硬脂酸甘油酯等；(8)吸附剂，如高岭土等；和(9)润滑剂，如滑石、硬脂酸钙、硬脂酸镁、固体聚乙二醇、十二烷基硫酸钠等，或其混合物。胶囊剂、片剂和丸剂中也可包含缓冲剂。The compounds of the present invention or pharmaceutically acceptable salts thereof can be formulated into solid dosage forms for oral administration, including but not limited to capsules, tablets, pills, powders, granules, and the like. In these solid dosage forms, the compounds of formula (I) of the present invention are mixed as active ingredient with at least one conventional inert excipient (or carrier), such as sodium citrate or dicalcium phosphate, or with the following ingredients: (1 ) fillers or compatibilizers, such as starch, lactose, sucrose, glucose, mannitol and silicic acid, etc.; (2) binders, such as hydroxymethyl cellulose, alginate, gelatin, polyvinylpyrrolidone, sucrose and arabino glue, etc.; (3) humectants, such as glycerin, etc.; (4) disintegrating agents, such as agar, calcium carbonate, potato starch or tapioca starch, alginic acid, some complex silicates and sodium carbonate, etc.; (5) slow Solvents, such as paraffin, etc.; (6) Absorption accelerators, such as quaternary ammonium compounds, etc.; (7) Wetting agents, such as cetyl alcohol and glycerol monostearate, etc.; (8) Adsorbents, such as kaolin, etc.; and (9) ) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycol, sodium lauryl sulfate, etc., or mixtures thereof. Buffers may also be included in capsules, tablets and pills.
所述固体剂型如片剂、糖丸、胶囊剂、丸剂和颗粒剂可采用包衣和壳材料例如肠溶衣和其他本领域公知的材料进行包衣或微囊化。它们可包含不透明剂，并且这种组合物中活性成分的释放可以延迟的方式在消化道内的某一部分中释放。可采用的包埋组分的实例是聚合物质和蜡类物质。必要时、活性成分也可与上述赋形剂中的一种或多种形成微胶囊形式。The solid dosage forms such as tablets, dragees, capsules, pills and granules can be coated or microencapsulated with coatings and shell materials such as enteric coatings and other materials well known in the art. They may contain opacifying agents, and the release of the active ingredient in such compositions may be in a certain part of the digestive tract in a delayed manner. Examples of embedding components that can be employed are polymeric substances and waxes. If desired, the active ingredient may also be in microencapsulated form with one or more of the above-mentioned excipients.
本发明化合物或其药学上可接受的盐可以配制为用于口服给药的液体剂型，包括但不限于药学上可接受的乳液、溶液、悬浮液、糖浆和酊剂等。除了作为活性成分的式(I)化合物或其药学上可接受的盐外，液体剂型可包含本领域中常规采用的惰性稀释剂如水和其他溶剂、增溶剂和乳化剂，如乙醇、异丙醇、碳酸乙酯、乙酸乙酯、丙二醇、1、3-丁二醇、二甲基甲酰胺以及油类，特别是棉籽油、花生油、玉米胚油、橄榄油、蓖麻油和芝麻油等或这些物质的混合物等。除了这些惰性稀释剂外，本发明液体剂型也可包含常规助剂，如润湿剂、乳化剂和悬浮剂、甜味剂、矫味剂和香料等。The compounds of the present invention, or pharmaceutically acceptable salts thereof, may be formulated in liquid dosage forms for oral administration, including, but not limited to, pharmaceutically acceptable emulsions, solutions, suspensions, syrups, tinctures, and the like. In addition to the compound of formula (I) or a pharmaceutically acceptable salt thereof as the active ingredient, liquid dosage forms may contain inert diluents conventionally employed in the art such as water and other solvents, solubilizers and emulsifiers such as ethanol, isopropanol , ethyl carbonate, ethyl acetate, propylene glycol, 1,3-butanediol, dimethylformamide and oils, especially cottonseed oil, peanut oil, corn germ oil, olive oil, castor oil and sesame oil or the like mixture, etc. Besides these inert diluents, the liquid dosage forms of the present invention may also contain conventional adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring and perfuming agents, and the like.
所述悬浮剂包括如乙氧基化异十八烷醇、聚氧乙烯山梨醇和脱水山梨醇只、微晶纤维素、甲醇铝和琼脂等或这些物质的混合物。Such suspending agents include, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan only, microcrystalline cellulose, aluminum methoxide and agar, and the like or mixtures of these substances.
本发明化合物或其药学上可接受的盐可以配制为用于肠胃外注射的剂型包括但不限于生理上可接受的无菌含水或无水溶液、分散液、悬浮液或乳液，以及用于重新溶解成无菌的可注射溶液或分散液的无菌粉末。适宜的载体、稀释剂、溶剂或赋形剂包括水、乙醇、多元醇及其适宜的混合物。The compounds of the present invention, or pharmaceutically acceptable salts thereof, can be formulated in dosage forms for parenteral injection including, but not limited to, physiologically acceptable sterile aqueous or anhydrous solutions, dispersions, suspensions or emulsions, and for reconstitution Sterile powder for sterile injectable solution or dispersion. Suitable carriers, diluents, solvents or excipients include water, ethanol, polyols and suitable mixtures thereof.
本发明化合物或其药学上可接受的盐也可以配制为用于局部给药的剂型包括如软膏剂、散剂、栓剂、滴剂、喷射剂和吸入剂等。作为活性成分的本发明式(I)化合物或其药学上可接受的盐在无菌条件下和生理上可接受的载体及任选的防腐剂、缓冲剂，或必要时可能需要的推进剂一起混合。The compounds of the present invention, or pharmaceutically acceptable salts thereof, may also be formulated for topical administration in dosage forms including, for example, ointments, powders, suppositories, drops, propellants, inhalants, and the like. The compound of formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, as the active ingredient is under sterile conditions together with a physiologically acceptable carrier and optionally a preservative, buffer, or propellant which may be required if necessary mix.
本发明还提供药物组合物，它含有本发明式(I)化合物或其药学上可接受的盐作为活性成分，以及药学上可接受载体、赋形剂或稀释剂。在制备药物组合物时，通常是将本发明式(I)化合物或其药学上可接受的盐与药学上可接受载体、赋形剂或稀释剂混合。The present invention also provides a pharmaceutical composition comprising a compound of formula (I) of the present invention or a pharmaceutically acceptable salt thereof as an active ingredient, and a pharmaceutically acceptable carrier, excipient or diluent. In preparing a pharmaceutical composition, the compound of formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, is usually admixed with a pharmaceutically acceptable carrier, excipient or diluent.
可以按常规制备方法将所述本发明组合物配制为常规药物制剂。例如片剂、丸剂、胶囊剂、散剂、颗粒剂、乳液剂、混浮剂、分散液、溶液剂、糖浆剂、酏剂、软膏剂、滴剂、栓剂、吸入剂、喷射剂等。The compositions of the present invention can be formulated into conventional pharmaceutical preparations according to conventional preparation methods. For example, tablets, pills, capsules, powders, granules, emulsions, suspensions, dispersions, solutions, syrups, elixirs, ointments, drops, suppositories, inhalants, propellants, and the like.
本发明所述的化合物或其药学上可接受的盐可以单独给药，或者(如果需要)与其他药学上可接受的治疗剂联合给药，如与其他抗肿瘤药物。待组合的各成分可同时或顺序的给予，以单一制剂形式或以不同制剂的形式给予。所述组合不仅可包括本发明化合物和一种其他活性剂的组合，也可包括本发明化合物和两种或更多种其他活性剂的组合。The compounds of the present invention, or pharmaceutically acceptable salts thereof, can be administered alone, or (if desired) in combination with other pharmaceutically acceptable therapeutic agents, such as other antineoplastic agents. The ingredients to be combined may be administered simultaneously or sequentially, in a single formulation or in separate formulations. The combination may include not only a combination of a compound of the present invention and one other active agent, but also a combination of a compound of the present invention and two or more other active agents.
本发明中，可与SOS1降解剂式(I)化合物一起或组合使用的其他药学上可接受的治疗剂可为：EGFR和/或其突变体抑制剂、ErbB2(Her2)和/或其突变体抑制剂、ALK和/或其突变体抑制剂、MEK和/或其突变体抑制剂、Kras和/或其突变体抑制剂、BCR-ABL和/或其突变体抑制剂、FGFR1/FGFR2/FGFR3和/或其突变体抑制剂、ROS1和/或其突变体抑制剂、c-MET和/或其突变体抑制剂、AXL和/或其突变体抑制剂、NTRK1和/或其突变体抑制剂、RET和/或其突变体抑制剂、紫杉烷、含铂化合物、抗代谢物、有丝分裂激酶抑制剂、免疫治疗剂、抗血管生成药物、拓扑异构酶抑制剂、A-Raf/B-Raf/C-RAf和/或其突变体抑制剂、ERK和/或其突变体抑制剂、细胞凋亡抑制剂、mTOR抑制剂、外遗传调控剂、IGF1/2和/或IGF1-R抑制剂、Ras GEF和/或其突变体抑制剂、PI3K和/或其突变体抑制剂。In the present invention, other pharmaceutically acceptable therapeutic agents that can be used together or in combination with the SOS1 degrading agent formula (I) compound can be: EGFR and/or its mutant inhibitors, ErbB2 (Her2) and/or its mutants Inhibitor, ALK and/or its mutant inhibitor, MEK and/or its mutant inhibitor, Kras and/or its mutant inhibitor, BCR-ABL and/or its mutant inhibitor, FGFR1/FGFR2/FGFR3 and/or its mutant inhibitors, ROS1 and/or its mutant inhibitors, c-MET and/or its mutant inhibitors, AXL and/or its mutant inhibitors, NTRK1 and/or its mutant inhibitors , RET and/or mutant inhibitors, taxanes, platinum-containing compounds, antimetabolites, mitotic kinase inhibitors, immunotherapeutics, antiangiogenic drugs, topoisomerase inhibitors, A-Raf/B- Raf/C-RAf and/or its mutant inhibitors, ERK and/or its mutant inhibitors, apoptosis inhibitors, mTOR inhibitors, epigenetic modulators, IGF1/2 and/or IGF1-R inhibitors , Ras GEF and/or mutant inhibitors thereof, PI3K and/or mutant inhibitors thereof.
本发明中，可与SOS1降解剂式(I)化合物一起或组合使用的其他药学上可接受的治疗剂可为：阿法替尼(afatinib)、厄洛替尼(erlotinib)、吉非替尼(gefitinib)、拉帕替尼(lapatinib)、西妥昔单抗、帕尼单抗、奥希替尼、奥莫替尼(olmutinib)、EGF-816、、曲妥珠单抗(trastuzumab)、帕妥珠单抗(pertuzumab)、唑替尼(crizotinib)、阿雷替尼(alectinib)、恩曲替尼(entrectinib)、布吉替尼(brigatinib)、曲美替尼(trametinib)、考比替尼(cobimetinib)、贝美替尼(binimetinib)、司美替尼(selumetinib)、瑞法替尼(refametinib)、伊马替尼(imatinib)、达沙替尼(dasatinib)、尼罗替尼(nilotinib)、尼达尼布(nintedanib)、克唑替尼、劳拉替尼(lorlatinib)、色瑞替尼(ceritinib)、美乐替尼(merestinib)、紫杉醇(paclitaxel)、nab-紫杉醇、多西他赛(docetaxel)、顺铂(cisplatin)、卡铂(carboplatin)、奥沙利铂(oxaliplatin)、5-氟尿嘧啶、卡培他滨(capecitabine)、氟尿苷、阿糖胞苷(cytarabine)、吉西他滨(gemcitabine)、曲氟尿苷(trifluridine)及替比嘧啶(tipiracil)的组合(＝TAS102)、帕博西尼(palbociclib)、瑞博西尼(ribociclib)、阿贝西尼(abemaciclib)、伊匹单抗(ipilimumab)、纳武单抗(nivolumab)、帕博利珠单抗(pembrolizumab)、阿替珠单抗(atezolizumab)、阿维鲁单抗(avelumab)、德瓦鲁单抗(durvalumab)、匹利珠单抗(pidilizumab)、PDR-001(＝斯帕珠单抗(spartalizumab))、贝伐珠单抗(bevacizumab)、伊立替康(irinotecan)、脂质体伊立替康、托泊替康(topotecan)、乌利替尼(ulixertinib)、雷帕霉素、替西罗莫司(temsirolimus)、依维莫司(everolimus)、利达莫司(ridaforolimus)、JQ-1、GSK 525762、OTX 015(＝MK8628)、CPI 0610、TEN-010(＝RO6870810)、珍妥珠单抗(xentuzumab)(WO 2010/066868中的抗体60833)或MEDI-573(＝杜昔妥单抗(dusigitumab))。In the present invention, other pharmaceutically acceptable therapeutic agents that can be used together or in combination with the SOS1 degrader compound of formula (I) can be: afatinib, erlotinib, gefitinib (gefitinib), lapatinib, cetuximab, panitumumab, osimertinib, olmutinib, EGF-816, trastuzumab, Pertuzumab, crizotinib, alectinib, entrectinib, brigatinib, trametinib, cobiratinib Cobimetinib, binimetinib, selumetinib, refametinib, imatinib, dasatinib, nilotinib ( nilotinib, nintedanib, crizotinib, lorlatinib, ceritinib, merestinib, paclitaxel, nab-paclitaxel, multiple Docetaxel, cisplatin, carboplatin, oxaliplatin, 5-fluorouracil, capecitabine, floxuridine, cytarabine , combination of gemcitabine, trifluridine and tipiracil (=TAS102), palbociclib, ribociclib, abemaciclib , ipilimumab, nivolumab, pembrolizumab, atezolizumab, avelumab, durvalumab ( durvalumab), pidilizumab, PDR-001 (=spartalizumab), bevacizumab, irinotecan, liposomal irinotecan, Topotecan, ulixertinib, rapamycin, temsirolimus, everolimus, lidalimus aforolimus), JQ-1, GSK 525762, OTX 015 (=MK8628), CPI 0610, TEN-010 (=RO6870810), xentuzumab (antibody 60833 in WO 2010/066868) or MEDI-573 (=dusigitumab).
本发明通过SOS1激酶活性测试实验证明本发明所述式Ⅰ化合物能够有效的与SOS1靶蛋白结合或产生抑制效果，通过Western-Blot证明本发明所述式Ⅰ化合物能够有效的特异性的降解NCI-H358细胞中SOS1蛋白。本发明所述式Ⅰ化合物，和/其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、代谢物、前药和/或其药学上可接受的盐可有效的降解SOS1蛋白，从而达到预防或治疗与SOS1相关或与SOS1与Ras或者SOS1与Rac相互作用所引起的疾病或病症的效果。In the present invention, the SOS1 kinase activity test experiment proves that the compound of formula I of the present invention can effectively bind to SOS1 target protein or produce an inhibitory effect, and Western-Blot proves that the compound of formula I of the present invention can effectively and specifically degrade NCI- SOS1 protein in H358 cells. The compound of formula I of the present invention, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, metabolites, prodrugs and/or pharmaceutically acceptable compounds thereof The acceptable salt can effectively degrade the SOS1 protein, so as to achieve the effect of preventing or treating diseases or disorders caused by the interaction of SOS1 or SOS1 and Ras or SOS1 and Rac.
具体实施方式Detailed ways
下面将结合实施例对本发明做进一步详细、完整地说明，但决非限制本发明，本发明也并非仅局限于实施例的内容。本发明实施例中的起始原料是已知的并且可以在市场上买到、或者可以采用或按照本领域已知的方法来合成。在无特殊说明的情况下，本发明实施例中未注明具体条件的实验方法，通常按照常规条件，或按照原料或商品制造厂商所建议的条件。The present invention will be further described in detail and completely below in conjunction with the embodiments, but the present invention is by no means limited, and the present invention is not limited to the contents of the embodiments. The starting materials in the examples of the present invention are known and commercially available, or can be synthesized using or according to methods known in the art. Unless otherwise specified, the experimental methods for which specific conditions are not indicated in the examples of the present invention are generally based on conventional conditions or conditions suggested by raw material or commodity manufacturers.
Ⅰ化合物制备实施例Ⅰ Compound Preparation Example
中间体1：(R)-1-(3-硝基-5-(三氟甲基)苯基)乙基-1-胺盐酸盐的制备Intermediate 1: Preparation of (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl-1-amine hydrochloride
步骤1：1-(3-硝基-5-(三氟甲基)苯基)乙基-1-酮的制备Step 1: Preparation of 1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl-1-one
Figure PCTCN2022088560-appb-000538
Figure PCTCN2022088560-appb-000538
氮气保护下，1-溴-3-硝基-5-(三氟甲基)苯(18g，66.7mmol)，三丁基(1-乙氧基乙烯基)锡烷(31g，86.7mmol)，Pd(PPh 3) 2Cl 2(4.7g，6.67mmol)和TEA(13.5g，133mmol)在1,4-二氧六环(200mL)溶液中的反应混合物于80℃下搅拌反应过夜。反应液用氟化钾(饱和水溶液，300mL)淬灭，并用EA(200mL×3)萃取。收集有机层并减压浓缩。将浓缩物溶解在THF(180mL)中，加入盐酸(100mL，6M)后，在室温下搅拌3h。然后将混合物用水(300mL)淬灭，并用EA(200mL×3)萃取。收集有机层，并用无水硫酸钠干燥，过滤并减压浓缩。粗产 Under nitrogen, 1-bromo-3-nitro-5-(trifluoromethyl)benzene (18 g, 66.7 mmol), tributyl(1-ethoxyvinyl)stannane (31 g, 86.7 mmol), A reaction mixture of Pd( PPh3 ) 2Cl2 (4.7 g , 6.67 mmol) and TEA (13.5 g, 133 mmol) in 1,4-dioxane (200 mL) was stirred at 80 °C overnight. The reaction solution was quenched with potassium fluoride (saturated aqueous solution, 300 mL), and extracted with EA (200 mL×3). The organic layer was collected and concentrated under reduced pressure. The concentrate was dissolved in THF (180 mL), and hydrochloric acid (100 mL, 6M) was added, followed by stirring at room temperature for 3 h. The mixture was then quenched with water (300 mL) and extracted with EA (200 mL x 3). The organic layer was collected, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. rough production
物经柱层析纯化得到目标产物1-(3-硝基-5-(三氟甲基)苯基)乙基-1-酮。The compound was purified by column chromatography to obtain the target product 1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl-1-one.
1H NMR(400MHz,CDCl 3)δ8.95(t,J＝1.6Hz,1H),8.69(s,1H),8.54(d,J＝0.5Hz,1H),2.76(s,3H). 1 H NMR (400 MHz, CDCl 3 ) δ 8.95 (t, J=1.6 Hz, 1H), 8.69 (s, 1H), 8.54 (d, J=0.5 Hz, 1H), 2.76 (s, 3H).
步骤2：(R,E)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)亚乙基)丙基-2-亚磺酰胺的制备Step 2: Preparation of (R,E)-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethylidene)propyl-2-sulfinamide
Figure PCTCN2022088560-appb-000539
Figure PCTCN2022088560-appb-000539
1-(3-硝基-5-(三氟甲基)苯基)乙基-1-酮(10.6g，45.5mmol)，(R)-2-甲基丙基-2-亚磺酰胺(8.3g，68.2mmol)和钛酸四乙酯(25.9g，114mmol)在THF(200mL)溶液中的反应混合物于60℃下搅拌反应2h。用水(300mL)淬灭反应混合物，并用EA(200mL×3)萃取溶液。收集有机层并用无水硫酸钠干燥，过滤并在减压下浓缩。浓缩物经柱层析纯化得到目标产物(R,E)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)亚乙基)丙基-2-亚磺酰胺。1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl-1-one (10.6 g, 45.5 mmol), (R)-2-methylpropyl-2-sulfinamide ( A reaction mixture of 8.3 g, 68.2 mmol) and tetraethyl titanate (25.9 g, 114 mmol) in THF (200 mL) was stirred at 60 °C for 2 h. The reaction mixture was quenched with water (300 mL), and the solution was extracted with EA (200 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain the target product (R,E)-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethylene)propyl- 2-Sulfinamide.
1H NMR(400MHz,DMSO-d 6)δ8.87(s,1H),8.61(s,1H),8.43(s,1H),2.90(s,3H),1.37(s,9H). 1 H NMR (400MHz, DMSO-d 6 ) δ 8.87(s,1H), 8.61(s,1H), 8.43(s,1H), 2.90(s,3H), 1.37(s,9H).
步骤3：(R)-2-甲基-N-((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)丙基-2-亚磺酰胺的制备Step 3: (R)-2-methyl-N-((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)propyl-2-sulfinamide preparation
Figure PCTCN2022088560-appb-000540
Figure PCTCN2022088560-appb-000540
向(R,E)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)亚乙基)丙基-2-亚磺酰胺(10g,30.7mmol)在THF(100mL)和水(20mL)溶液中的混合物中加入NaBH 4(1.28g,33.7mmol)。反应混合物在-10℃下搅拌反应1分钟后用水(300mL)淬灭反应混合物，并用EA(200mL×3)萃取溶液。收集有机层并用无水硫酸钠干燥，过滤并减压浓缩。浓缩物经柱柱层析纯化得到目标产物(R)-2-甲基-N-((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基) 丙基-2-亚磺酰胺。 To (R,E)-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethylidene)propyl-2-sulfinamide (10 g, 30.7 mmol) to a mixture of a solution of THF (100 mL) and water ( 20 mL) was added NaBH4 (1.28 g, 33.7 mmol). The reaction mixture was stirred at -10°C for 1 min after which the reaction mixture was quenched with water (300 mL) and the solution was extracted with EA (200 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain the target product (R)-2-methyl-N-((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)propane yl-2-sulfinamide.
1H NMR(400MHz,CDCl 3)δ8.45–8.42(m,2H),7.96(s,1H),4.76–4.68(m,1H),3.56(d,J＝4.2Hz,1H),1.62(d,J＝6.7Hz,3H),1.26(s,9H). 1 H NMR (400MHz, CDCl 3 ) δ 8.45-8.42 (m, 2H), 7.96 (s, 1H), 4.76-4.68 (m, 1H), 3.56 (d, J=4.2Hz, 1H), 1.62 ( d, J=6.7Hz, 3H), 1.26(s, 9H).
步骤4：(R)-1-(3-硝基-5-(三氟甲基)苯基)乙基-1-胺盐酸盐的制备Step 4: Preparation of (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl-1-amine hydrochloride
Figure PCTCN2022088560-appb-000541
Figure PCTCN2022088560-appb-000541
将(R)-2-甲基-N-((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)丙基-2-亚磺酰胺(5.5g，16.3mmol)置于盐酸(80mL,4M)二氧六环溶液中，并于25℃下搅拌反应2h。过滤粗产物，并用石油醚(100mL)洗涤，得到目标产物(R)-1-(3-硝基-5-(三氟甲基)苯基)乙基-1-胺盐酸盐。(R)-2-methyl-N-((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)propyl-2-sulfinamide (5.5 g , 16.3 mmol) was placed in a solution of hydrochloric acid (80 mL, 4 M) in dioxane, and the reaction was stirred at 25 °C for 2 h. The crude product was filtered and washed with petroleum ether (100 mL) to give the target product (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl-1-amine hydrochloride.
LC-MS:(ESI,m/z):[M+H] +＝235.2. LC-MS: (ESI, m/z): [M+H] + = 235.2.
中间体2：4-(4,4,5,5-四甲基-1,3,2-二噁硼戊环-2-基)环己-3-烯-1-羧酸乙酯Intermediate 2: 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaboropenan-2-yl)cyclohex-3-ene-1-carboxylate ethyl ester
步骤1：4-(((三氟甲基)磺酰基)氧基)环己-3-烯-1-羧酸乙酯的制备Step 1: Preparation of ethyl 4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000542
Figure PCTCN2022088560-appb-000542
在0℃下，向搅拌的4-氧代基环己烷-1-甲酸乙酯(5g，32.0mmol)和2,6-二甲基吡啶(4.6g，42.9mmol)在DCM(60mL)中的混合物中滴加Tf 2O(9g，32.0mmol)。反应混合物在0℃下搅拌反应1h。然后将反应混合物在25℃下搅拌反应15分钟，并加入Tf 2O(7g，25.6mmol)。然后将反应混合物在25℃下搅拌过夜。浓缩反应混合物，用水(300mL)淬灭反应，并用EA(200mL×3)萃取。收集有机层，并用无水硫酸钠干燥，过滤并减压浓缩。浓缩物经柱层析纯化得到4-(((三氟甲基)磺酰基)氧基)环己-3-烯-1-羧酸乙酯。 To a stirred solution of ethyl 4-oxocyclohexane-1-carboxylate (5 g, 32.0 mmol) and 2,6-lutidine (4.6 g, 42.9 mmol) in DCM (60 mL) at 0 °C Tf2O ( 9 g, 32.0 mmol) was added dropwise to the mixture. The reaction mixture was stirred at 0 °C for 1 h. The reaction mixture was then stirred at 25°C for 15 minutes and Tf2O ( 7 g, 25.6 mmol) was added. The reaction mixture was then stirred at 25°C overnight. The reaction mixture was concentrated, quenched with water (300 mL), and extracted with EA (200 mL x 3). The organic layer was collected, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain ethyl 4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate.
1H NMR(400MHz,DMSO-d 6)δ5.90(d,J＝3.9Hz,1H),4.14–4.02(m,2H),2.68–2.60(m,1H),2.47–2.27(m,4H),2.08–1.98(m,1H),1.88–1.76(m,1H),1.19(t,J＝7.1Hz,3H). 1 H NMR (400MHz, DMSO-d 6 )δ5.90(d, J=3.9Hz, 1H), 4.14-4.02(m, 2H), 2.68-2.60(m, 1H), 2.47-2.27(m, 4H) ), 2.08–1.98 (m, 1H), 1.88–1.76 (m, 1H), 1.19 (t, J=7.1Hz, 3H).
步骤2：4-(4,4,5,5-四甲基-1,3,2-二噁硼戊环-2-基)环己-3-烯-1-羧酸乙酯的制备Step 2: Preparation of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylic acid ethyl ester
Figure PCTCN2022088560-appb-000543
Figure PCTCN2022088560-appb-000543
4-(((三氟甲基)磺酰基)氧基)环己-3-烯-1-羧酸乙酯(4.7g,16.8mmol)，(Bpin) 2(6.4g,25.2mmol)，Pd(dppf) 2Cl 2(1.2g,1.68mmol)和KOAc(4.9g,50.4mmol)在1，4-二氧六环(80mL)溶液中的混合物于90℃下搅拌反应过夜。用水(300mL)淬灭反应，并用EA(200mL×3)萃取。收集有机层，并用无水硫酸钠干燥，过滤并减压浓缩。浓缩物物经柱层析纯化得到4-(4,4,5,5-四甲基-1,3,2-二噁硼戊环-2-基)环己-3-烯-1-羧酸乙酯。 Ethyl 4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate (4.7g, 16.8mmol), (Bpin) 2 (6.4g, 25.2mmol), Pd A mixture of (dppf)2Cl2 ( 1.2 g , 1.68 mmol) and KOAc (4.9 g, 50.4 mmol) in 1,4-dioxane (80 mL) was stirred at 90 °C overnight. The reaction was quenched with water (300 mL) and extracted with EA (200 mL x 3). The organic layer was collected, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropenan-2-yl)cyclohex-3-ene-1-carboxylate ethyl acetate.
1H NMR(400MHz,DMSO-d 6)δ6.42(d,J＝2.2Hz,1H),4.11-4.02(m,2H),2.33-1.95(m,4H),1.93-1.83(m,1H),1.53-1.38(m,1H),1.21-1.14(m,16H). 1 H NMR (400MHz, DMSO-d 6 ) δ 6.42 (d, J=2.2Hz, 1H), 4.11-4.02 (m, 2H), 2.33-1.95 (m, 4H), 1.93-1.83 (m, 1H) ),1.53-1.38(m,1H),1.21-1.14(m,16H).
中间体3：((1R,4R)-4-(4-(((R)-1-(3-氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮Intermediate 3: ((1R,4R)-4-(4-(((R)-1-(3-amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone
步骤1：2-氨基-5-溴-4-甲氧基苯甲酸的制备Step 1: Preparation of 2-amino-5-bromo-4-methoxybenzoic acid
Figure PCTCN2022088560-appb-000544
Figure PCTCN2022088560-appb-000544
0℃下，向搅拌的2-氨基-4-甲氧基苯甲酸(30g,179mmol)的DMF(600mL)溶液中加入NBS(35g,197mmol)，反应混合物在25℃下搅拌反应1h。反应液用硫代硫酸钠(饱和水溶液，500mL)淬灭，并用EA(500mL×3)萃取。收集有机层，并用氯化钠(饱和水溶液，500mL×3)洗涤，无水硫酸钠干燥，过滤并浓缩，得到2-氨基-5-溴-4-甲氧基苯甲酸粗产物，粗产物无需进一步纯化即可直接用于下一步。To a stirred solution of 2-amino-4-methoxybenzoic acid (30 g, 179 mmol) in DMF (600 mL) was added NBS (35 g, 197 mmol) at 0 °C, and the reaction mixture was stirred at 25 °C for 1 h. The reaction solution was quenched with sodium thiosulfate (saturated aqueous solution, 500 mL), and extracted with EA (500 mL×3). The organic layer was collected, washed with sodium chloride (saturated aqueous solution, 500 mL×3), dried over anhydrous sodium sulfate, filtered and concentrated to obtain crude 2-amino-5-bromo-4-methoxybenzoic acid, which was unnecessary Further purification can be used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝246.0. LC-MS: (ESI, m/z): [M+H] + = 246.0.
步骤2：6-溴-7-甲氧基-2-甲基喹唑啉-4(3H)-酮的制备Step 2: Preparation of 6-bromo-7-methoxy-2-methylquinazolin-4(3H)-one
Figure PCTCN2022088560-appb-000545
Figure PCTCN2022088560-appb-000545
向搅拌的2-氨基-5-溴-4-甲氧基苯甲酸(17.0g,69.1mmol)的甲醇(170mL)溶液中加入乙酸铵(53.2g,691mmol)和原乙酸三甲酯(83.0g,691mmol)。所得反应混合物在密闭容器中于120℃下搅拌反应24h。反应混合物倒入水(1L)中，并将固体产物过滤。用EA(1L)洗涤粗产物，得到目标产物6-溴-7-甲氧基-2-甲基喹唑啉-4(3H)-酮。粗产物无需纯化即可直接用于下一步反应。To a stirred solution of 2-amino-5-bromo-4-methoxybenzoic acid (17.0 g, 69.1 mmol) in methanol (170 mL) was added ammonium acetate (53.2 g, 691 mmol) and trimethyl orthoacetate (83.0 g) , 691 mmol). The resulting reaction mixture was stirred in a closed vessel at 120°C for 24h. The reaction mixture was poured into water (1 L) and the solid product was filtered. The crude product was washed with EA (1 L) to give the desired product 6-bromo-7-methoxy-2-methylquinazolin-4(3H)-one. The crude product was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝268.9. LC-MS: (ESI, m/z): [M+H] + = 268.9.
步骤3：6-溴-4-氯-7-甲氧基-2-甲基喹唑啉的制备Step 3: Preparation of 6-bromo-4-chloro-7-methoxy-2-methylquinazoline
Figure PCTCN2022088560-appb-000546
Figure PCTCN2022088560-appb-000546
6-溴-7-甲氧基-2-甲基喹唑啉-4(3H)-酮(10g,37.2mmol)在三氯氧磷(200mL)溶液中的混合物在105℃下搅拌过夜。将反应混合物浓缩，用碳酸氢钠(饱和水溶液，500mL)淬灭，并用EA(300mL×3)萃取。收集有机层，并用无水硫酸钠干燥，过滤并浓缩。浓缩物经硅胶柱层析纯化，得到目标产物6-溴-4-氯-7-甲氧基-2-甲基喹唑啉。A mixture of 6-bromo-7-methoxy-2-methylquinazolin-4(3H)-one (10 g, 37.2 mmol) in phosphorous oxychloride (200 mL) was stirred at 105 °C overnight. The reaction mixture was concentrated, quenched with sodium bicarbonate (saturated aqueous solution, 500 mL), and extracted with EA (300 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the target product 6-bromo-4-chloro-7-methoxy-2-methylquinazoline.
LC-MS:(ESI,m/z):[M+H] +＝287.0. LC-MS: (ESI, m/z): [M+H] + = 287.0.
步骤4：(R)-6-溴-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺的制备Step 4: (R)-6-Bromo-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)quinazoline Preparation of -4-amine
Figure PCTCN2022088560-appb-000547
Figure PCTCN2022088560-appb-000547
向6-溴-4-氯-7-甲氧基-2-甲基喹唑啉(1.8g,6.27mmol)在EtOH(12mL)溶液中混合物中加入(R)-1-(3-硝基-5-(三氟甲基))苯基)乙基-1-胺盐酸盐(1.7g,7.52mmol)和DIEA(1.6g,12.5mmol)。将反应混合物在微波中于100℃搅拌反应5h。用水(300mL)淬灭反应，并用EA(300mL×3)萃取。收集有机层，并用经无水硫酸钠干燥，过滤并减压浓缩。浓缩物经柱层析纯化得到黄色油状(R)-6-溴-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺。To a mixture of 6-bromo-4-chloro-7-methoxy-2-methylquinazoline (1.8 g, 6.27 mmol) in EtOH (12 mL) was added (R)-1-(3-nitro -5-(Trifluoromethyl))phenyl)ethyl-1-amine hydrochloride (1.7 g, 7.52 mmol) and DIEA (1.6 g, 12.5 mmol). The reaction mixture was stirred in the microwave at 100 °C for 5 h. The reaction was quenched with water (300 mL) and extracted with EA (300 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to give (R)-6-bromo-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl) as yellow oil )ethyl)quinazolin-4-amine.
LC-MS:(ESI,m/z):[M+H] +＝484.9. LC-MS: (ESI, m/z): [M+H] + = 484.9.
步骤5：4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己-3-烯-1-羧酸乙酯的制备Step 5: 4-(7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinoline Preparation of oxazolin-6-yl)cyclohex-3-ene-1-carboxylic acid ethyl ester
Figure PCTCN2022088560-appb-000548
Figure PCTCN2022088560-appb-000548
将(R)-6-溴-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺(2g,4.12mmol)，4-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)环己-3-烯-1-羧酸乙酯(2.31g,8.24mmol)，碳酸钠(873mg,8.24mmol)和Pd(dppf) 2Cl 2(300mg,0.41mmol)在DMF(24mL)和水(3mL)中的反应混合物于110℃搅拌反应过夜。用水(300mL)淬灭反应。EA(300mL×3)萃取溶液，并用氯化钠(饱和的水溶液,500mL×3)洗涤，合并有机层。有机层经无水硫酸钠干燥，过滤并减压浓缩。浓缩物经柱层析纯化得到4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己-3-烯-1-羧酸乙酯。 (R)-6-Bromo-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)quinazoline-4 -amine (2g, 4.12mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboran-2-yl)cyclohex-3-ene-1-carboxylate A reaction mixture of ethyl acetate (2.31 g, 8.24 mmol), sodium carbonate (873 mg, 8.24 mmol) and Pd(dppf)2Cl2 ( 300 mg , 0.41 mmol) in DMF (24 mL) and water (3 mL) at 110 °C The reaction was stirred overnight. The reaction was quenched with water (300 mL). The solution was extracted with EA (300 mL×3) and washed with sodium chloride (saturated aqueous solution, 500 mL×3), and the organic layers were combined. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to give 4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethane) yl)amino)quinazolin-6-yl)cyclohex-3-ene-1-carboxylate ethyl ester.
LC-MS:(ESI,m/z):[M+H] +＝559.7. LC-MS: (ESI, m/z): [M+H] + = 559.7.
步骤6：(R)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-1-羧酸乙酯的制备Step 6: (R)-4-(4-((1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazole Preparation of ethyl lino-6-yl)cyclohexyl-1-carboxylate
Figure PCTCN2022088560-appb-000549
Figure PCTCN2022088560-appb-000549
向4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己-3-烯-1-羧酸乙酯(1.7g,3.04mmol)在MeOH(60mL)溶液中的混合物中加入Pd/C(1.02g,0.6w/w)。反应混合物在氢气氛围下于50℃搅拌反应4天。将粗产物过滤，得到(R)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-1-羧酸乙酯。to 4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline To a mixture of ethyl-6-yl)cyclohex-3-ene-1-carboxylate (1.7 g, 3.04 mmol) in MeOH (60 mL) was added Pd/C (1.02 g, 0.6 w/w). The reaction mixture was stirred at 50°C under a hydrogen atmosphere for 4 days. The crude product was filtered to give (R)-4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methyl ethyl quinazolin-6-yl)cyclohexyl-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝531.2. LC-MS: (ESI, m/z): [M+H] + = 531.2.
步骤7：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7)甲氧基-2-甲基喹唑啉-6-基)环己烷-1-甲酸的制备Step 7: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7)methoxy- Preparation of 2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000550
Figure PCTCN2022088560-appb-000550
向(R)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸乙酯(1.5g,2.82mmol)在甲醇(8mL)，THF(8mL)和水(16mL)中的混合物中加入氢氧化锂(203mg,8.46mmol)。将反应混合物于60℃搅拌反应过夜。粗产物通过制备型HPLC纯化，得到(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7)甲氧基-2-甲基喹唑啉-6-基)环己烷-1-甲酸。To (R)-4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- To a mixture of ethyl 6-yl)cyclohexane-1-carboxylate (1.5 g, 2.82 mmol) in methanol (8 mL), THF (8 mL) and water (16 mL) was added lithium hydroxide (203 mg, 8.46 mmol) . The reaction mixture was stirred at 60°C overnight. The crude product was purified by preparative HPLC to give (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)- 7) Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝503.2. LC-MS: (ESI, m/z): [M+H] + = 503.2.
1H NMR(400MHz,DMSO-d 6)δ8.13(d,J＝8.0Hz,1H),8.06(s,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.69(s,1H),5.56(dd,J＝13.6,5.8Hz,3H),3.88(s,3H),2.92(t,J＝11.7Hz,1H),2.35(s,3H),2.24(t,J＝11.8Hz,1H),2.05(d,J＝10.8Hz,2H),1.87(d,J＝11.8Hz,2H),1.66–1.40(m,7H). 1 H NMR (400MHz, DMSO-d 6 )δ8.13(d, J=8.0Hz, 1H), 8.06(s, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.69(s, 1H), 5.56(dd, J=13.6, 5.8Hz, 3H), 3.88(s, 3H), 2.92(t, J=11.7Hz, 1H), 2.35(s, 3H), 2.24(t,J＝11.8Hz,1H),2.05(d,J＝10.8Hz,2H),1.87(d,J＝11.8Hz,2H),1.66–1.40(m,7H).
步骤8：4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7)甲氧基-2-甲基喹唑啉-6-基)环 己烷-1-羰基)哌嗪-1-羧酸叔丁酯Step 8: 4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7)methan Oxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000551
Figure PCTCN2022088560-appb-000551
向(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-甲酸(220mg,0.44mmol)在EA(12mL)溶液中的混合物中加入哌嗪-1-甲酸叔丁基酯(163mg,0.88mmol)，DIEA(169mg,1.31mmol)和T 3P(209mg,0.66mmol)。将反应混合物于0℃下搅拌3h。用水(100mL)淬灭反应，并用EA(100mL×3)萃取，收集有机层并用无水硫酸钠干燥，过滤并减压浓缩。浓缩物柱层析纯化，得到4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7)甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯。 To (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- To a mixture of methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (220 mg, 0.44 mmol) in EA (12 mL) was added piperazine-1-carboxylic acid tert-butyl ester (163 mg, 0.88 mmol) , DIEA (169 mg, 1.31 mmol) and T3P (209 mg, 0.66 mmol). The reaction mixture was stirred at 0 °C for 3 h. The reaction was quenched with water (100 mL) and extracted with EA (100 mL×3), the organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to give 4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino )-7) Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝671.3. LC-MS: (ESI, m/z): [M+H] + = 671.3.
1H NMR(400MHz,DMSO-d 6)δ8.19–8.07(m,2H),6.99(s,1H),6.86(d,J＝10.5Hz,2H),6.70(s,1H),5.56(dd,J＝16.7,9.3Hz,3H),3.89(s,3H),3.47(m,4H),3.32(m,4H),2.95(s,1H),2.67(s,1H),2.36(s,3H),1.83(d,J＝14.5Hz,4H),1.59(t,J＝22.3Hz,7H),1.41(s,9H). 1 H NMR (400MHz, DMSO-d 6 )δ8.19-8.07(m, 2H), 6.99(s, 1H), 6.86(d, J=10.5Hz, 2H), 6.70(s, 1H), 5.56( dd, J＝16.7, 9.3Hz, 3H), 3.89(s, 3H), 3.47(m, 4H), 3.32(m, 4H), 2.95(s, 1H), 2.67(s, 1H), 2.36(s ,3H),1.83(d,J＝14.5Hz,4H),1.59(t,J＝22.3Hz,7H),1.41(s,9H).
步骤9：((1R,4R)-4-(4-(((R)-1-(3-氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮的制备Step 9: ((1R,4R)-4-(4-(((R)-1-(3-amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Preparation of yl-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000552
Figure PCTCN2022088560-appb-000552
将4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7)甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯(220mg,0.33mmol)在乙酸乙酯盐酸(3M,10mL)溶液中的混合物于25℃下搅拌反应2h。浓缩反应物，得到((1R,4R)-4-(4-(((R)-1-(3-氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮，粗产物无需进一步纯化即可用于下一步反应。4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7)methoxy -2-Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester (220 mg, 0.33 mmol) in ethyl acetate hydrochloric acid (3M, 10 mL) The mixture was stirred at 25 °C for 2 h. The reaction was concentrated to give ((1R,4R)-4-(4-(((R)-1-(3-amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone, the crude product was used in the next reaction without further purification.
LC-MS:(ESI,m/z):[M+H] +＝571.2. LC-MS: (ESI, m/z): [M+H] + = 571.2.
中间体4：2-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌啶-4-基)乙醛Intermediate 4: 2-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperidin-4 - base) acetaldehyde
步骤1：2-(2,6-二氧代基哌啶-3-基)-5-氟异吲哚啉-1,3-二酮Step 1: 2-(2,6-Dioxopiperidin-3-yl)-5-fluoroisoindoline-1,3-dione
Figure PCTCN2022088560-appb-000553
Figure PCTCN2022088560-appb-000553
向4-氟邻苯二甲酸(5.52g,0.03mol)的乙酸(50mL)溶液中加入3-氨基哌啶-2,6-二酮盐酸盐(5.0g,0.03mol)和乙酸钾(8.8g,0.09mol)，反应混合物于120℃搅拌反应过夜，将反应混合物减压浓缩，浓缩物用水(100mL)稀释，在室温下搅拌30分钟，过滤，固体用水(50mL×2)洗涤。减压干燥得到产物。To a solution of 4-fluorophthalic acid (5.52 g, 0.03 mol) in acetic acid (50 mL) was added 3-aminopiperidine-2,6-dione hydrochloride (5.0 g, 0.03 mol) and potassium acetate (8.8 g, 0.09 mol), the reaction mixture was stirred at 120 °C overnight, the reaction mixture was concentrated under reduced pressure, the concentrate was diluted with water (100 mL), stirred at room temperature for 30 minutes, filtered, and the solid was washed with water (50 mL×2). The product was obtained by drying under reduced pressure.
LC-MS:(ESI,m/z):[M+H] +＝277.1 LC-MS: (ESI, m/z): [M+H] + = 277.1
步骤2：2-(2,6-二氧代基哌啶-3-基)-5-(4-(2-羟乙基)哌啶-1-基)异吲哚啉-1,3-二酮的制备Step 2: 2-(2,6-Dioxopiperidin-3-yl)-5-(4-(2-hydroxyethyl)piperidin-1-yl)isoindoline-1,3- Preparation of diketones
Figure PCTCN2022088560-appb-000554
Figure PCTCN2022088560-appb-000554
2-(2,6-二氧代基哌啶-3-基)-5-氟异吲哚啉-1,3-二酮(500mg,1.81mmol)，2-(哌啶-4-基)乙基-1-醇(280mg,2.17mmol))和DIEA(701mg,5.43mmol)在NMP(5mL)中的混合物于140℃的微波反应器中反应5小时。用水(50mL)稀释反应混合物，并用乙酸乙酯(50mL×2)萃取。收集有机相并用水(100mL×2)和饱和食盐水(50mL)洗涤，经无水硫酸钠干燥后，过滤并浓缩。浓缩物经硅胶柱上纯化，得到产物。2-(2,6-Dioxopiperidin-3-yl)-5-fluoroisoindoline-1,3-dione (500 mg, 1.81 mmol), 2-(piperidin-4-yl) A mixture of ethyl-1-ol (280 mg, 2.17 mmol)) and DIEA (701 mg, 5.43 mmol) in NMP (5 mL) was reacted in a microwave reactor at 140°C for 5 hours. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (50 mL x 2). The organic phase was collected and washed with water (100 mL×2) and saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified on a silica gel column to give the product.
LC-MS:(ESI,m/z):[M+H] +＝386.1. LC-MS: (ESI, m/z): [M+H] + = 386.1.
步骤3：2-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌啶-4-基)乙醛的制备Step 3: 2-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperidin-4- Preparation of acetaldehyde
Figure PCTCN2022088560-appb-000555
Figure PCTCN2022088560-appb-000555
2-(2,6-二氧代基哌啶-3-基)-5-(4-(2-羟乙基)哌啶-1-基)异吲哚啉-1,3-二酮(300mg,0.78mmol)和IBX(436mg,1.56mmol)在乙腈(6mL)中的混合物于80℃下搅拌反应2h。用水(30mL)稀释反应混合物，并用乙酸乙酯(30mL×2)萃取。收集有机相并用水(50mL×2)和饱和食盐水(30mL)洗涤，经无水硫酸钠干燥后，过滤并浓缩。浓缩物经通过硅胶柱层析纯化得到产物。2-(2,6-Dioxopiperidin-3-yl)-5-(4-(2-hydroxyethyl)piperidin-1-yl)isoindoline-1,3-dione ( A mixture of 300 mg, 0.78 mmol) and IBX (436 mg, 1.56 mmol) in acetonitrile (6 mL) was stirred at 80 °C for 2 h. The reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate (30 mL x 2). The organic phase was collected and washed with water (50 mL×2) and saturated brine (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the product.
LC-MS:(ESI,m/z):[M+H] +＝384.1. LC-MS: (ESI, m/z): [M+H] + = 384.1.
1H NMR(400MHz,DMSO-d 6)δ11.07(s,1H),9.69(t,J＝1.6Hz,1H),7.65(d,J＝8.6Hz,1H),7.31(d,J＝2.0Hz,1H),7.23(dd,J＝8.6,2.2Hz,1H),5.06(dd,J＝12.9,5.4Hz,1H),4.03(dd,J＝10.3,2.9Hz,2H),3.04–2.82(m,3H),2.65–2.52(m,2H),2.41(dd,J＝6.7,1.6Hz,2H),2.17–1.97(m,2H),1.73(d,J＝11.1Hz,2H),1.2-1.18(m,2H). 1H NMR (400MHz, DMSO-d 6 )δ11.07(s, 1H), 9.69(t, J=1.6Hz, 1H), 7.65(d, J=8.6Hz, 1H), 7.31(d, J=2.0 Hz, 1H), 7.23 (dd, J=8.6, 2.2Hz, 1H), 5.06 (dd, J=12.9, 5.4Hz, 1H), 4.03 (dd, J=10.3, 2.9Hz, 2H), 3.04–2.82 (m, 3H), 2.65–2.52 (m, 2H), 2.41 (dd, J=6.7, 1.6Hz, 2H), 2.17–1.97 (m, 2H), 1.73 (d, J=11.1Hz, 2H), 1.2-1.18(m,2H).
中间体5：2-(3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3-氮杂螺[5.5]十一烷-9-基)乙醛Intermediate 5: 2-(3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]deca Monoalk-9-yl)acetaldehyde
步骤1：4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸的制备Step 1: Preparation of 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid
Figure PCTCN2022088560-appb-000556
Figure PCTCN2022088560-appb-000556
将3-氨基-4-氯苯甲酸(5.0g,2.93mmol)悬浮于丙烯酸(8.05mL,117mmol)中，并在100℃下搅拌反应3h，然后将反应液搅拌冷却至室温。加入乙酸(33ml)，将搅拌的悬浮液在100℃加热10分钟，加入尿素(11.00g,183mmol)，反应液在120℃搅拌反应过夜。将反应液加入到冰水和浓盐酸(37％)的混合液中，搅拌，将得到的悬浮液在5℃的冰箱中保存过夜，然后过滤，固体用水洗涤并干燥，得到固体。将固体在盐酸溶液(0.05M)中研磨，过滤，甲基叔丁基醚洗涤，40℃下减压干燥，得到目标产物。3-Amino-4-chlorobenzoic acid (5.0 g, 2.93 mmol) was suspended in acrylic acid (8.05 mL, 117 mmol), and the reaction was stirred at 100° C. for 3 h, and then the reaction solution was stirred and cooled to room temperature. Acetic acid (33 ml) was added, the stirred suspension was heated at 100°C for 10 minutes, urea (11.00 g, 183 mmol) was added, and the reaction was stirred at 120°C overnight. The reaction solution was added to a mixture of ice water and concentrated hydrochloric acid (37%), stirred, and the resulting suspension was stored in a refrigerator at 5°C overnight, then filtered, and the solid was washed with water and dried to obtain a solid. The solid was triturated in hydrochloric acid solution (0.05M), filtered, washed with methyl tert-butyl ether, and dried under reduced pressure at 40°C to give the desired product.
LC-MS:(ESI,m/z):[M+H] +＝269.0 LC-MS: (ESI, m/z): [M+H] + = 269.0
步骤2：4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯的制备Step 2: Preparation of pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate
Figure PCTCN2022088560-appb-000557
Figure PCTCN2022088560-appb-000557
4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸(2.0g,7.58mmol)，2,3,4,5,6-五氟苯酚(1.67g,9.09mmol)和N,N'-二环己基碳酰亚胺(1.87g,9.09mmol)在N,N-二甲基甲酰胺(20mL)溶液中的混合物在室温 下搅拌反应3h。将反应液倒入水(200mL)中并搅拌0.5h，溶液用乙酸乙酯(200mL×3)萃取。收集有机相，并用水(500mL×2)和饱和食盐水(300mL)洗涤，用无水硫酸钠干燥，过滤并浓缩。浓缩物经硅胶柱层析纯化，得到目标产物。4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid (2.0 g, 7.58 mmol), 2,3,4,5,6-pentafluorophenol ( A mixture of 1.67 g, 9.09 mmol) and N,N'-dicyclohexylcarbonimide (1.87 g, 9.09 mmol) in N,N-dimethylformamide (20 mL) was stirred at room temperature for 3 h. The reaction solution was poured into water (200 mL) and stirred for 0.5 h, and the solution was extracted with ethyl acetate (200 mL×3). The organic phase was collected, washed with water (500 mL×2) and saturated brine (300 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝435.0 LC-MS: (ESI, m/z): [M+H] + = 435.0
步骤3：2-(3-氮杂[5.5]十一烷-9-基)乙-1-醇的制备Step 3: Preparation of 2-(3-aza[5.5]undecan-9-yl)ethan-1-ol
Figure PCTCN2022088560-appb-000558
Figure PCTCN2022088560-appb-000558
向9-(2-羟乙基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(1.0g,3mmol)在EA(10mL)溶液中的混合物中加如Pd(OH) 2/C(200mg)，反应混合物在氢气氛围下于室温下搅拌反应16h。过滤混合物，浓缩滤液，得到目标产物。 To a mixture of benzyl 9-(2-hydroxyethyl)-3-azaspiro[5.5]undecane-3-carboxylate (1.0 g, 3 mmol) in EA (10 mL) was added a solution such as Pd(OH). ) 2 /C (200 mg), the reaction mixture was stirred at room temperature for 16 h under a hydrogen atmosphere. The mixture was filtered and the filtrate was concentrated to give the desired product.
步骤4：1-(2-氯-5-(9-(2-羟乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(2-Chloro-5-(9-(2-hydroxyethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4( Preparation of 1H,3H)-dione
Figure PCTCN2022088560-appb-000559
Figure PCTCN2022088560-appb-000559
向2-(3-氮杂螺[5.5]十一烷-9-基)乙-1-醇(500mg,2.5mmol)在DMSO(5mL)溶液中的混合物中加入4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯基酯(1.0g,2.5mmol)和DIEA(0.5mL)。用水(30mL)淬灭反应，并用EA(10mL×3)萃取。收集有机层并用水(10mL×2)和饱和食盐水(10mL)洗涤，用无水硫酸钠干燥，过滤并浓缩。浓缩物经柱层析纯化，得到目标化合物。To a mixture of 2-(3-azaspiro[5.5]undecan-9-yl)ethan-1-ol (500 mg, 2.5 mmol) in DMSO (5 mL) was added 4-chloro-3-(2 , 4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester (1.0 g, 2.5 mmol) and DIEA (0.5 mL). The reaction was quenched with water (30 mL) and extracted with EA (10 mL x 3). The organic layer was collected and washed with water (10 mL×2) and saturated brine (10 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by column chromatography to obtain the target compound.
LC-MS:(ESI,m/z):[M+H] +＝448.1 LC-MS: (ESI, m/z): [M+H] + = 448.1
步骤5：2-(3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3-氮杂螺[5.5]十一烷-9-基)乙醛的制备Step 5: 2-(3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane Preparation of Alk-9-yl)acetaldehyde
Figure PCTCN2022088560-appb-000560
Figure PCTCN2022088560-appb-000560
向1-(2-氯-5-(9-(2-羟乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(700mg,1.56mmol)在THF(12mL)溶液中的混合物中加入IBX(873mg,3.1mmol)。反应混合物于80℃搅拌反应2h。用水(30mL)淬灭反应，并用EA(10mL×3)萃取溶液。收集有机层并用水(10mL×2)和饱和食盐盐水(10mL)洗涤，用无水硫酸钠干燥，过滤并浓缩。浓缩物经柱层析纯化，得到目标化合物。To 1-(2-chloro-5-(9-(2-hydroxyethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H, 3H)-dione (700 mg, 1.56 mmol) in THF (12 mL) was added IBX (873 mg, 3.1 mmol). The reaction mixture was stirred at 80 °C for 2 h. The reaction was quenched with water (30 mL), and the solution was extracted with EA (10 mL x 3). The organic layer was collected and washed with water (10 mL×2) and saturated brine (10 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by column chromatography to obtain the target compound.
LC-MS:(ESI,m/z):[M+H] +＝446.1 LC-MS: (ESI, m/z): [M+H] + = 446.1
中间体6：2-(4-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌嗪-1-基)乙醛Intermediate 6: 2-(4-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperazine-1 - base) acetaldehyde
步骤1：4-(2,2-二甲氧基乙基)哌嗪-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(2,2-dimethoxyethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000561
Figure PCTCN2022088560-appb-000561
向哌嗪-1-羧酸叔丁酯(2.0g,10.75mmol)，碳酸钾(4.45g,32.26mmol)和碘化钾(892mg,5.38mmol)的丙酮(20mL)混合物中加入2-溴-1,1-二甲氧基乙烷(3.63g,21.51mmol)。并于80℃下搅拌反应过夜。反应液混合物减压下浓缩。将浓缩物溶解在乙酸乙酯(50mL)中，并用水(50mL×2)和饱和食盐水(50mL)洗涤。收集有机相，有机相经无水硫酸钠干燥，过滤并浓缩。浓缩物经硅胶柱层析纯化，得到所需产物。To a mixture of piperazine-1-carboxylate tert-butyl ester (2.0 g, 10.75 mmol), potassium carbonate (4.45 g, 32.26 mmol) and potassium iodide (892 mg, 5.38 mmol) in acetone (20 mL) was added 2-bromo-1, 1-Dimethoxyethane (3.63 g, 21.51 mmol). The reaction was stirred at 80°C overnight. The reaction mixture was concentrated under reduced pressure. The concentrate was dissolved in ethyl acetate (50 mL), and washed with water (50 mL×2) and saturated brine (50 mL). The organic phase was collected, dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the desired product.
LC-MS:(ESI,m/z):[M+H] +＝275.0. LC-MS: (ESI, m/z): [M+H] + = 275.0.
步骤2：1-(2,2-二甲氧基乙基)哌嗪的制备Step 2: Preparation of 1-(2,2-dimethoxyethyl)piperazine
Figure PCTCN2022088560-appb-000562
Figure PCTCN2022088560-appb-000562
4-(2,2-二甲氧基乙基)哌嗪-1-羧酸叔丁酯(2.2g,8.03mmol)在盐酸/二氧六烷(4M,10mL)溶液中的混合物室温下搅拌过夜。减压浓缩得到目标产物(1.5g,粗品)。粗产物直接用于下一步。A mixture of tert-butyl 4-(2,2-dimethoxyethyl)piperazine-1-carboxylate (2.2 g, 8.03 mmol) in hydrochloric acid/dioxane (4M, 10 mL) was stirred at room temperature overnight. Concentration under reduced pressure gave the target product (1.5 g, crude). The crude product was used directly in the next step.
步骤3：5-(4-(2,2-二甲氧基乙基)哌嗪-1-基)-2-(2,6-二氧代基哌啶-3-基)异吲哚啉-1,3-二酮的制备Step 3: 5-(4-(2,2-Dimethoxyethyl)piperazin-1-yl)-2-(2,6-dioxopiperidin-3-yl)isoindoline Preparation of -1,3-dione
Figure PCTCN2022088560-appb-000563
Figure PCTCN2022088560-appb-000563
2-(2,6-二氧代基哌啶-3-基)-5-氟异吲哚啉-1,3-二酮(1.48g,5.36mmol)，1-(2,2-二甲氧基乙基)哌嗪(1.4g,8.05mmol)和DIEA(4.15g,36.16mmol)的NMP(10mL)溶液的混合物在微波反应器中140℃反应5h。用水(50mL)稀释混合物，并用乙酸乙酯(50mL×2)萃取。收集有机相并用水(100mL×2)和饱和食盐水(50mL)洗涤，经无水硫酸钠干燥，过滤并浓缩。浓缩物经硅胶柱层析纯化，得到目标产物。2-(2,6-Dioxopiperidin-3-yl)-5-fluoroisoindoline-1,3-dione (1.48g, 5.36mmol), 1-(2,2-dimethyl A mixture of oxyethyl)piperazine (1.4 g, 8.05 mmol) and DIEA (4.15 g, 36.16 mmol) in NMP (10 mL) was reacted in a microwave reactor at 140 °C for 5 h. The mixture was diluted with water (50 mL) and extracted with ethyl acetate (50 mL x 2). The organic phase was collected and washed with water (100 mL×2) and saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝431.1. LC-MS: (ESI, m/z): [M+H] + = 431.1.
步骤4：2-(4-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌嗪-1-基)乙醛的制备Step 4: 2-(4-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperazine-1- Preparation of acetaldehyde
Figure PCTCN2022088560-appb-000564
Figure PCTCN2022088560-appb-000564
5-(4-(2,2-二甲氧基乙基)哌嗪-1-基)-2-(2,6-二氧代基哌啶-3-基)异吲哚啉-1,3-二酮(1.8g,4.19mmol)在三氟乙酸/二氯甲烷(5mL/5mL)溶液中的混合物于室温下搅拌反应60h。减压浓缩混合物，加入水，并用碳酸氢钠(水溶液)将pH调节至8。混合物用乙酸乙酯(100mL×2)萃取。收集有机相，并用水(100mL×2)和饱和食盐水(100mL)洗涤，无水硫酸钠干燥，过滤并浓缩。浓缩物经硅胶柱上纯化，得到目标产物。5-(4-(2,2-Dimethoxyethyl)piperazin-1-yl)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1, A mixture of 3-diketone (1.8 g, 4.19 mmol) in trifluoroacetic acid/dichloromethane (5 mL/5 mL) solution was stirred at room temperature for 60 h. The mixture was concentrated under reduced pressure, water was added, and the pH was adjusted to 8 with sodium bicarbonate (aq). The mixture was extracted with ethyl acetate (100 mL×2). The organic phase was collected, washed with water (100 mL×2) and saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified on a silica gel column to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝385.0. LC-MS: (ESI, m/z): [M+H] + = 385.0.
中间体7：2-(9-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3,9-二氮杂螺[5.5]十一烷-3-基)乙醛Intermediate 7: 2-(9-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3,9-diazaspiro[ 5.5] Undecyl-3-yl)acetaldehyde
步骤1：9-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: 9-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3,9-diazaspiro[5.5]undecane Preparation of tert-butyl alkane-3-carboxylate
Figure PCTCN2022088560-appb-000565
Figure PCTCN2022088560-appb-000565
在室温，氮气保护下，向3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸(1.0g,3.78mmol)的N,N-二甲基甲酰胺(10mL)溶液中加入HATU(1.66g,4.37mmol)，3,9-二氮杂螺[5.5]十一烷基-3-羧酸叔丁酯(0.96g,3.78mmol)和N-甲基吗啡啉(0.8g,7.92mmol)。搅拌反应2h后，将反应混合物用水(50mL)淬灭，并用乙酸乙酯(50mL×3)萃取。收集有机层，并用饱和食盐水(50mL×3)洗涤，无水硫酸钠干燥，过滤并浓缩。浓缩物硅胶柱层析纯化，得到目标产物。To a solution of 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid (1.0 g, 3.78 mmol) in N,N- To a solution of dimethylformamide (10 mL) was added HATU (1.66 g, 4.37 mmol), tert-butyl 3,9-diazaspiro[5.5]undecyl-3-carboxylate (0.96 g, 3.78 mmol) and N-methylmorpholine (0.8 g, 7.92 mmol). After stirring the reaction for 2 h, the reaction mixture was quenched with water (50 mL) and extracted with ethyl acetate (50 mL x 3). The organic layer was collected, washed with saturated brine (50 mL×3), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝505.2 LC-MS: (ESI, m/z): [M+H] + = 505.2
步骤2：1-(2-氯-5-(3,9-二氮杂螺[5.5]十一烷基-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Chloro-5-(3,9-diazaspiro[5.5]undecyl-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dihydropyrimidine Preparation of ketones
Figure PCTCN2022088560-appb-000566
Figure PCTCN2022088560-appb-000566
9-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.56g,3.1mmol)在三氟乙酸/二氯甲烷(2.5mL/5mL)溶液中的反应液于室温搅拌反应4h。将反应液减压浓缩，得到目标化合物粗产物。粗产物直接用于下一步反应。9-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3,9-diazaspiro[5.5]undecan-3 - The reaction solution of tert-butyl carboxylate (1.56 g, 3.1 mmol) in trifluoroacetic acid/dichloromethane (2.5 mL/5 mL) solution was stirred at room temperature for 4 h. The reaction solution was concentrated under reduced pressure to obtain a crude product of the target compound. The crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝405.1 LC-MS: (ESI, m/z): [M+H] + = 405.1
步骤3：1-(2-氯-5-(9-(2,2-二甲氧基乙基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(9-(2,2-dimethoxyethyl)-3,9-diazaspiro[5.5]undecan-3-carbonyl)phenyl) Preparation of dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000567
Figure PCTCN2022088560-appb-000567
向1-(2-氯-5-(3,9-二氮杂螺[5.5]十一烷基-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(200mg,0.25mmol)，碳酸钾(155mg,1.25mmol)和碘化钾(19mg,0.11mmol)在丙酮(4mL)溶液中的混合物中加入2-溴-1,1-二甲氧基乙烷(46mg,0.3mmol)。反应液在80℃下搅拌反应3h，随后减压浓缩。浓缩物硅胶柱层析纯化，得到目标化合物。To 1-(2-chloro-5-(3,9-diazaspiro[5.5]undecyl-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione ( 200 mg, 0.25 mmol), potassium carbonate (155 mg, 1.25 mmol) and potassium iodide (19 mg, 0.11 mmol) in acetone (4 mL) were added 2-bromo-1,1-dimethoxyethane (46 mg, 0.3 mmol). The reaction solution was stirred at 80 °C for 3 h, and then concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography to obtain the target compound.
LC-MS:(ESI,m/z):[M+H] +＝493.3. LC-MS: (ESI, m/z): [M+H] + = 493.3.
步骤4：2-(9-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3,9-二氮杂螺[5.5]十一烷-3-基)乙醛的制备Step 4: 2-(9-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3,9-diazaspiro[5.5 Preparation of ]undecan-3-yl)acetaldehyde
Figure PCTCN2022088560-appb-000568
Figure PCTCN2022088560-appb-000568
将1-(2-氯-5-(9-(2,2-二甲氧基乙基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(121mg,0.246mmol)在三氟乙酸/二氯甲烷(1mL/2mL)溶液中的混合物于室温搅拌反应4小时。减压浓缩反应液。浓缩物硅胶柱层析纯化，得到目标化合物。1-(2-Chloro-5-(9-(2,2-dimethoxyethyl)-3,9-diazaspiro[5.5]undecan-3-carbonyl)phenyl)dihydro A mixture of pyrimidine-2,4(1H,3H)-dione (121 mg, 0.246 mmol) in trifluoroacetic acid/dichloromethane (1 mL/2 mL) solution was stirred at room temperature for 4 hours. The reaction solution was concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography to obtain the target compound.
LC-MS:(ESI,m/z):[M+H] +＝447.1. LC-MS: (ESI, m/z): [M+H] + = 447.1.
中间体8：3-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌啶-4-基)丙醛Intermediate 8: 3-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperidin-4 -yl) propionaldehyde
步骤1：2-(2,6-二氧代基哌啶-3-基)-5-(4-(3-羟丙基)哌啶-1-基)异吲哚啉-1,3-二酮的制备Step 1: 2-(2,6-Dioxopiperidin-3-yl)-5-(4-(3-hydroxypropyl)piperidin-1-yl)isoindoline-1,3- Preparation of diketones
Figure PCTCN2022088560-appb-000569
Figure PCTCN2022088560-appb-000569
2-(2,6-二氧代基哌啶-3-基)-5-氟异吲哚啉-1,3-二酮(500mg,1.81mmol)，3-(哌啶-4-基)丙基-1-醇(310mg,2.17mmol))和DIEA(701mg,5.43mmol)在NMP(5mL)中的混合物于140℃的微波反应器中反应5小时。用水(50mL)稀释反应混合物，并用乙酸乙酯(50mL×2)萃取。收集有机相并用水(100mL×2)和饱和食盐水(50mL)洗涤，经无水硫酸钠干燥后，过滤并浓缩。浓缩物经硅胶柱上纯化，得到目标产物。2-(2,6-Dioxopiperidin-3-yl)-5-fluoroisoindoline-1,3-dione (500 mg, 1.81 mmol), 3-(piperidin-4-yl) A mixture of propyl-1-ol (310 mg, 2.17 mmol)) and DIEA (701 mg, 5.43 mmol) in NMP (5 mL) was reacted in a microwave reactor at 140°C for 5 hours. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (50 mL x 2). The organic phase was collected and washed with water (100 mL×2) and saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified on a silica gel column to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝400.2. LC-MS: (ESI, m/z): [M+H] + = 400.2.
步骤2：3-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-5-基)哌啶-4-基)丙醛的制备Step 2: 3-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)piperidin-4- Preparation of yl) propionaldehyde
Figure PCTCN2022088560-appb-000570
Figure PCTCN2022088560-appb-000570
2-(2,6-二氧代基哌啶-3-基)-5-(4-(3-羟丙基)哌啶-1-基)异吲哚啉-1,3-二酮的(310mg,0.78mmol)和IBX(436mg,1.56mmol)在乙腈(6mL)中的混合物于80℃下搅拌反应2h。用水(30mL)稀释反应混合物，并用乙酸乙酯(30mL×2)萃取。收集有机相并用水(50mL×2)和饱和食盐水(30mL)洗涤，经无水硫酸钠干燥后，过滤并浓缩。浓缩物经硅胶柱层析纯化得到产物。2-(2,6-Dioxopiperidin-3-yl)-5-(4-(3-hydroxypropyl)piperidin-1-yl)isoindoline-1,3-dione A mixture of (310 mg, 0.78 mmol) and IBX (436 mg, 1.56 mmol) in acetonitrile (6 mL) was stirred at 80 °C for 2 h. The reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate (30 mL x 2). The organic phase was collected and washed with water (50 mL×2) and saturated brine (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by silica gel column chromatography to obtain the product.
LC-MS:(ESI,m/z):[M+H] +＝398.2. LC-MS: (ESI, m/z): [M+H] + = 398.2.
中间体9：(R)-N-(1-(3-氨基-5-(三氟甲基)苯基)乙基)-7-甲氧基-2-甲基-6-(哌啶-4-基)喹唑啉-4-胺Intermediate 9: (R)-N-(1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)-7-methoxy-2-methyl-6-(piperidine- 4-yl)quinazolin-4-amine
步骤1：2-氨基-5-溴-4-甲氧基苯甲酸的制备Step 1: Preparation of 2-amino-5-bromo-4-methoxybenzoic acid
Figure PCTCN2022088560-appb-000571
Figure PCTCN2022088560-appb-000571
在0℃下，向搅拌的2-氨基-4-甲氧基苯甲酸(16.7g,100.0mmol)的DMF(300mL)溶液中加入NBS(19.6g,110.0mmol)。反应混合物于25℃下搅拌反应1h，并用水(300mL)淬灭反应，用EA(300mL×3)萃取，收集有机层，并用氯化钠(饱和的水溶液,300mL×3)洗涤，无水硫酸铵干燥并浓缩，得到目标粗产物。粗产物无需纯化直接用于下一步反应。To a stirred solution of 2-amino-4-methoxybenzoic acid (16.7 g, 100.0 mmol) in DMF (300 mL) at 0 °C was added NBS (19.6 g, 110.0 mmol). The reaction mixture was stirred at 25 °C for 1 h, and quenched with water (300 mL), extracted with EA (300 mL×3), the organic layer was collected, washed with sodium chloride (saturated aqueous solution, 300 mL×3), anhydrous sulfuric acid The ammonium was dried and concentrated to give the desired crude product. The crude product was used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝247.4. LC-MS: (ESI, m/z): [M+H] + = 247.4.
步骤2：6-溴-7-甲氧基-2-甲基喹唑啉-4-醇的制备Step 2: Preparation of 6-bromo-7-methoxy-2-methylquinazolin-4-ol
Figure PCTCN2022088560-appb-000572
Figure PCTCN2022088560-appb-000572
向2-氨基-5-溴-4-甲氧基苯甲酸(19.5g,79.3mmol)在MeOH(195mL)溶液中的混合物中加入醋酸铵(61.0g,793mmol)和原乙酸三甲酯(95.1g,793mmol)。反应混合物在密闭容器中于120℃搅拌反应24小时。将反应混合物倒入水(500mL)中，并将固体产物过滤。粗产物用EA洗涤得到目标粗产物，粗产物无需纯化直接用于下一步反应。To a mixture of 2-amino-5-bromo-4-methoxybenzoic acid (19.5 g, 79.3 mmol) in MeOH (195 mL) was added ammonium acetate (61.0 g, 793 mmol) and trimethyl orthoacetate (95.1 g, 793 mmol). The reaction mixture was stirred in a closed vessel at 120°C for 24 hours. The reaction mixture was poured into water (500 mL) and the solid product was filtered. The crude product was washed with EA to obtain the target crude product, and the crude product was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝271.0. LC-MS: (ESI, m/z): [M+H] + = 271.0.
步骤3：4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯的制备Step 3: Preparation of 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylic acid tert-butyl ester
Figure PCTCN2022088560-appb-000573
Figure PCTCN2022088560-appb-000573
向6-溴-7-甲氧基-2-甲基喹唑啉-4-醇(1.5g,3.09mmol)在DMF(30mL)和水(4mL)混合溶液中的混合物中加入4-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁基(1.73g,6.18mmol)，碳酸钠(982mg,9.27mmol)和Pd(dppf) 2Cl 2(226mg,0.319mmol)。反应混合物在110℃下搅拌反应过夜。用水(300mL)淬灭反应混合物，并用EA(200mL×3)萃取，收集有机层，有机层经无水硫酸钠干燥并减压浓缩。浓缩物经柱层析纯化，得到目标产物。 To a mixture of 6-bromo-7-methoxy-2-methylquinazolin-4-ol (1.5 g, 3.09 mmol) in a mixed solution of DMF (30 mL) and water (4 mL) was added 4-(4 ,4,5,5-Tetramethyl-1,3,2-dioxaboran-2-yl)-3,6-dihydropyridine-1(2H)-carboxylic acid tert-butyl (1.73g, 6.18 mmol), sodium carbonate (982 mg, 9.27 mmol) and Pd(dppf)2Cl2 ( 226 mg , 0.319 mmol). The reaction mixture was stirred at 110°C overnight. The reaction mixture was quenched with water (300 mL) and extracted with EA (200 mL×3), the organic layer was collected, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝372.2. LC-MS: (ESI, m/z): [M+H] + = 372.2.
步骤4：4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000574
Figure PCTCN2022088560-appb-000574
向4-(4-羟基-7-甲氧基喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯(500mg,0.894mmol)的MeOH(20mL)溶液中加入Pd/C(300mg)。反应混合物在50℃下H 2氛围下搅拌反应2天。反应液经硅藻土过滤，滤液减压浓缩得到目标产物4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯。粗品直接用于下一步反应。 To 4-(4-hydroxy-7-methoxyquinazolin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylate tert-butyl ester (500 mg, 0.894 mmol) in MeOH (20 mL) ) solution was added Pd/C (300 mg). The reaction mixture was stirred for 2 days at 50 °C under H2 atmosphere. The reaction solution was filtered through celite, and the filtrate was concentrated under reduced pressure to obtain the target product 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)piperidine-1-carboxylate tert-butyl ester . The crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝374.2. LC-MS: (ESI, m/z): [M+H] + = 374.2.
步骤5：4-(7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯的制备Step 5: 4-(7-Methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl)piperidine Preparation of tert-butyl pyridine-1-carboxylate
Figure PCTCN2022088560-appb-000575
Figure PCTCN2022088560-appb-000575
向4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯(250.0mg,0.76mmol)，TPSCl(295.0mg,1.0mmol),DMAP(13.0mg,0.1mmol)的DCM(5.0mL)溶液中加入TEA(0.3mL,2.4mmol)。反应混合物在室温下搅拌反应12h。反应液用DCM稀释，饱和NaHCO 3溶液洗。有机相用Na 2SO 4干燥，过滤，浓缩。所得粗品经柱层析(洗脱剂体系为EA/PE)纯化得到产物4-(7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯。 To tert-butyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)piperidine-1-carboxylate (250.0 mg, 0.76 mmol), TPSCl (295.0 mg, 1.0 mmol), DMAP (13.0 mg, 0.1 mmol) in DCM (5.0 mL) was added TEA (0.3 mL, 2.4 mmol). The reaction mixture was stirred at room temperature for 12 h. The reaction solution was diluted with DCM and washed with saturated NaHCO 3 solution. The organic phase was dried over Na2SO4 , filtered and concentrated. The obtained crude product was purified by column chromatography (the eluent system was EA/PE) to obtain the product 4-(7-methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl) )sulfonyl)oxy)quinazolin-6-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝640.0. LC-MS: (ESI, m/z): [M+H] + = 640.0.
步骤6：(R)-4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯的制备Step 6: (R)-4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinoline Preparation of oxazolin-6-yl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000576
Figure PCTCN2022088560-appb-000576
向4-(7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯(400mg,0.03mmol)的DMSO(8mL)溶液中加入(R)-1-(3-硝基-5-(三氟甲基)苯基)乙-1-胺盐酸盐(203mg,0.75mmol)和TEA(0.8mL)。反应混合物在90℃下搅拌反应过夜。反应用水淬灭，EA萃取。有机相用Na 2SO 4干燥，过滤，浓缩。所得粗品经正向柱纯化得到目标产物(R)-4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯。 To 4-(7-methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl)piperidine- To a solution of tert-butyl 1-carboxylate (400 mg, 0.03 mmol) in DMSO (8 mL) was added (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethan-1-amine salt acid (203 mg, 0.75 mmol) and TEA (0.8 mL). The reaction mixture was stirred at 90°C overnight. The reaction was quenched with water and extracted with EA. The organic phase was dried over Na2SO4 , filtered and concentrated. The obtained crude product was purified by forward column to obtain the target product (R)-4-(7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl) )ethyl)amino)quinazolin-6-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝590.3. LC-MS: (ESI, m/z): [M+H] + = 590.3.
步骤7：(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺的制备Step 7: (R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine- Preparation of 4-yl)quinazolin-4-amine
Figure PCTCN2022088560-appb-000577
Figure PCTCN2022088560-appb-000577
向(R)-4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯(220mg,0.328mmol)的DCM溶液中加入TFA。反应混合物在25℃下搅拌反应2h。浓缩得到目标产物(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺。所得粗品直接用于下一步反应。To (R)-4-(7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline To a solution of -6-yl)piperidine-1-carboxylate tert-butyl ester (220 mg, 0.328 mmol) in DCM was added TFA. The reaction mixture was stirred at 25 °C for 2 h. Concentrated to obtain the target product (R)-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine) -4-yl)quinazolin-4-amine. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝490.2 LC-MS: (ESI, m/z): [M+H] + = 490.2
步骤8：(R)-N-(1-(3-氨基-5-(三氟甲基)苯基)乙基)-7-甲氧基-2-甲基-6-(哌啶-4-基)喹唑啉-4-胺的制备Step 8: (R)-N-(1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)-7-methoxy-2-methyl-6-(piperidine-4 -Preparation of quinazolin-4-amine
Figure PCTCN2022088560-appb-000578
Figure PCTCN2022088560-appb-000578
向(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺(124mg,0.25mmol)的EtOH/H 2O(3mL/1ml)溶液中加入NH 4Cl(135.6mg,2.5mmol)和Fe粉(141.5mg,2.5mmol)。反应混合物在70℃下N 2氛围下搅拌反应2h。反应液过滤，浓缩得到粗品。粗品经制备HPLC纯化得到目标产物(R)-N-(1-(3-氨基-5-(三氟甲基)苯基)乙基)-7-甲氧基-2-甲基-6-(哌啶-4-基)喹唑啉-4-胺。 To (R)-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine-4- yl)quinazolin-4-amine (124 mg, 0.25 mmol) in EtOH/H 2 O (3 mL/1 ml) was added NH 4 Cl (135.6 mg, 2.5 mmol) and Fe powder (141.5 mg, 2.5 mmol). The reaction mixture was stirred at 70 °C under N2 atmosphere for 2 h. The reaction solution was filtered and concentrated to obtain crude product. The crude product was purified by preparative HPLC to give the target product (R)-N-(1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)-7-methoxy-2-methyl-6- (Piperidin-4-yl)quinazolin-4-amine.
LC-MS:(ESI,m/z):[M+H] +＝460.2. LC-MS: (ESI, m/z): [M+H] + = 460.2.
1H NMR(400MHz,DMSO-d 6)δ8.32(s,1H),8.09(s,1H),7.03(s,1H),6.88(d,J＝11.1Hz,1H),6.70(s,1H),5.57(d,J＝6.9Hz,1H),3.89(s,3H),3.39–3.25(m,2H),3.22–3.13(m,1H),3.07–2.95(m,2H),2.36(s,3H),2.03–1.85(m,4H),1.56(d,J＝7.0Hz,3H). 1 H NMR (400MHz, DMSO-d 6 ) δ 8.32(s, 1H), 8.09(s, 1H), 7.03(s, 1H), 6.88(d, J=11.1Hz, 1H), 6.70(s, 1H), 5.57(d, J＝6.9Hz, 1H), 3.89(s, 3H), 3.39-3.25(m, 2H), 3.22-3.13(m, 1H), 3.07-2.95(m, 2H), 2.36 (s, 3H), 2.03–1.85 (m, 4H), 1.56 (d, J=7.0Hz, 3H).
中间体10：(R)-N-(1-(3-氨基-5-(三氟甲基)苯基)乙基)-7-甲氧基-2-甲基-6-(哌啶-4-氧基)喹唑啉-4-胺Intermediate 10: (R)-N-(1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)-7-methoxy-2-methyl-6-(piperidine- 4-Oxy)quinazolin-4-amine
步骤1：4-((甲磺酰基)氧基)哌啶-1-羧酸叔丁酯Step 1: tert-Butyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000579
Figure PCTCN2022088560-appb-000579
在0℃下，往4-羟基哌啶-1-羧酸叔丁酯(10.0g,49.7mmol)和TEA(15.0g,149.1mmol)在DCM(100mL)溶液中的混合物中滴加溶于DCM(20.0mL)溶液中的甲磺酰氯(7.4g,64.9mmol)。反应混合物于室温下搅拌反应过夜，然后加入水(200mL)，用DCM(200mL×2)萃取，收集有机层，饱和食盐水洗涤，无水硫酸钠干燥并减压浓缩，浓缩物经柱层析纯化得目标产物。To a mixture of tert-butyl 4-hydroxypiperidine-1-carboxylate (10.0 g, 49.7 mmol) and TEA (15.0 g, 149.1 mmol) in DCM (100 mL) at 0°C was added dropwise a solution of 4-hydroxypiperidine-1-carboxylate in DCM (20.0 mL) methanesulfonyl chloride (7.4 g, 64.9 mmol) in solution. The reaction mixture was stirred at room temperature overnight, then water (200 mL) was added, extracted with DCM (200 mL×2), the organic layer was collected, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure, and the concentrate was subjected to column chromatography The target product was purified.
LC-MS:(ESI,m/z):[M+H] +＝280.1. LC-MS: (ESI, m/z): [M+H] + = 280.1.
步骤2：6,7-二甲氧基-2-甲基喹唑啉-4-醇的制备Step 2: Preparation of 6,7-dimethoxy-2-methylquinazolin-4-ol
Figure PCTCN2022088560-appb-000580
Figure PCTCN2022088560-appb-000580
向2-氨基-4,5-二甲氧基苯甲酸(20.0g,0.1mol)在2-甲氧基乙醇(120.0mL)溶液中的混合物中加入盐酸乙脒(19.0g,0.2mol)和醋酸钠(16.4g,0.2mol)。反应混合物于140℃搅拌反应过夜。将反应混合物倒入水(250mL)中，并在室温下搅拌10min。然后将混合物过滤，滤饼用水洗涤，并将固体真空干燥，得到目标产物。To a solution of 2-amino-4,5-dimethoxybenzoic acid (20.0 g, 0.1 mol) in 2-methoxyethanol (120.0 mL) was added acetamidine hydrochloride (19.0 g, 0.2 mol) and Sodium acetate (16.4 g, 0.2 mol). The reaction mixture was stirred at 140°C overnight. The reaction mixture was poured into water (250 mL) and stirred at room temperature for 10 min. The mixture was then filtered, the filter cake was washed with water, and the solid was dried in vacuo to yield the desired product.
LC-MS:(ESI,m/z):[M+H] +＝221.2. LC-MS: (ESI, m/z): [M+H] + = 221.2.
步骤3：7-甲氧基-2-甲基喹唑啉-4,6-二醇的制备Step 3: Preparation of 7-methoxy-2-methylquinazoline-4,6-diol
Figure PCTCN2022088560-appb-000581
Figure PCTCN2022088560-appb-000581
将6,7-二甲氧基-2-甲基喹唑啉-4-醇(9.1g,41.4mmol)和DL-蛋氨酸(10.5g,70.4mmol)在甲磺酸(50mL)中的反应混合物在80℃下搅拌反应过夜。用冰水淬灭反应，并用氢氧化钠(2N)溶液碱化。滤出沉淀物，得到目标粗产物。A reaction mixture of 6,7-dimethoxy-2-methylquinazolin-4-ol (9.1 g, 41.4 mmol) and DL-methionine (10.5 g, 70.4 mmol) in methanesulfonic acid (50 mL) The reaction was stirred at 80°C overnight. The reaction was quenched with ice water and basified with sodium hydroxide (2N) solution. The precipitate was filtered off to obtain the desired crude product.
LC-MS:(ESI,m/z):[M+H] +＝207.2. LC-MS: (ESI, m/z): [M+H] + = 207.2.
步骤4：4-((4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 4-((4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)oxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000582
Figure PCTCN2022088560-appb-000582
将7-甲氧基-2-甲基喹唑啉-4,6-二醇(1.4g,6.8mmol)，4-((甲磺酰基)氧基)哌啶-1-羧酸叔丁酯(2.2g,8.2mmol)和碳酸钾(1.8g,13.6mmol)在NMP(10.0mL)溶液中的反应混合物于100℃下搅拌反应过夜。然后加入水(50.0mL)，并用EA(50mL×3)萃取，收集有机层，用饱和食盐水洗涤，无水硫酸钠干燥并减压浓缩，浓缩物经反相柱层析纯化(乙腈:水＝0-100％)得到目标产物。7-Methoxy-2-methylquinazoline-4,6-diol (1.4 g, 6.8 mmol), tert-butyl 4-((methylsulfonyl)oxy)piperidine-1-carboxylate A reaction mixture of (2.2 g, 8.2 mmol) and potassium carbonate (1.8 g, 13.6 mmol) in NMP (10.0 mL) was stirred at 100 °C overnight. Then water (50.0 mL) was added and extracted with EA (50 mL×3). The organic layer was collected, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was purified by reverse phase column chromatography (acetonitrile:water =0-100%) to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝390.2. LC-MS: (ESI, m/z): [M+H] + = 390.2.
步骤5：4-((7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯的制备Step 5: 4-((7-Methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl) Preparation of tert-butyl oxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000583
Figure PCTCN2022088560-appb-000583
将4-((4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯(800.0mg,2.0mmol)，2,4,6-三异丙基苯磺酰氯(748.0mg,2.4mmol)，DMAP(125.0mg,0.4mmol)和TEA(623.0mg,6.0mmol)在DCM(10.0mL)溶液中的反应混合物于室温下搅拌反应过夜。浓缩反应混合物，浓缩物经柱层析纯化，得到目标产物。4-((4-Hydroxy-7-methoxy-2-methylquinazolin-6-yl)oxy)piperidine-1-carboxylate tert-butyl ester (800.0 mg, 2.0 mmol), 2, A reaction mixture of 4,6-triisopropylbenzenesulfonyl chloride (748.0 mg, 2.4 mmol), DMAP (125.0 mg, 0.4 mmol) and TEA (623.0 mg, 6.0 mmol) in DCM (10.0 mL) at room temperature The reaction was stirred overnight. The reaction mixture was concentrated, and the concentrate was purified by column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+Na] +＝678.1. LC-MS: (ESI, m/z): [M+Na] + = 678.1.
步骤6：(R)-4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯的制备Step 6: (R)-4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) Preparation of quinazolin-6-yl)oxy)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000584
Figure PCTCN2022088560-appb-000584
将4-((7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯(0.8g,1.2mmol)，(R)-1-(3-硝基-5-(三氟甲基)苯基)乙-1-胺盐酸盐(0.43g,1.8mmol)和TEA(1.1g,10.8mmol)在DMSO(15.0mL)溶液中反应混合物于90℃下搅拌反应过夜。然后加入水(50.0mL)，并用EA(50mL×3)萃取，收集有机层，并用饱和食盐水洗涤，无水硫酸钠干燥并浓缩，浓缩物经反相柱层析纯化(乙腈-水＝0-100％)得到目标产物。4-((7-Methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl)oxy ) piperidine-1-carboxylate tert-butyl ester (0.8g, 1.2mmol), (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethan-1-amine hydrochloride (0.43 g, 1.8 mmol) and TEA (1.1 g, 10.8 mmol) in DMSO (15.0 mL) The reaction mixture was stirred at 90 °C overnight. Then water (50.0 mL) was added and extracted with EA (50 mL×3), the organic layer was collected, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated, and the concentrate was purified by reverse phase column chromatography (acetonitrile-water=0 -100%) to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝606.0. LC-MS: (ESI, m/z): [M+H] + = 606.0.
步骤7：(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-氧基)喹唑啉-4-胺的制备Step 7: (R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine- Preparation of 4-Oxy)quinazolin-4-amine
Figure PCTCN2022088560-appb-000585
Figure PCTCN2022088560-appb-000585
将(R)-4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羧酸叔丁酯(140mg,0.23mmol)在DCM(5.0mL)和TFA(1.0mL)溶液的混合物于室温下搅拌反应2.0h。减压浓缩反应物，得到(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-氧基)喹唑啉-4-胺。(R)-4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazole A mixture of tert-butyl lino-6-yl)oxy)piperidine-1-carboxylate (140 mg, 0.23 mmol) in DCM (5.0 mL) and TFA (1.0 mL) was stirred at room temperature for 2.0 h. The reaction was concentrated under reduced pressure to give (R)-7-methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6- (Piperidin-4-oxy)quinazolin-4-amine.
LC-MS:(ESI,m/z):[M+H] +＝506.1. LC-MS: (ESI, m/z): [M+H] + = 506.1.
步骤8：(R)-N-(1-(3-氨基-5-(三氟甲基)苯基)乙基)-7-甲氧基-2-甲基-6-(哌啶-4-氧基)喹唑啉-4-胺的制备Step 8: (R)-N-(1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)-7-methoxy-2-methyl-6-(piperidine-4 Preparation of -Oxy)quinazolin-4-amine
Figure PCTCN2022088560-appb-000586
Figure PCTCN2022088560-appb-000586
将(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-氧基)喹唑啉-4-胺(100.0mg,0.19mmol)和Pd/C(20.0mg)在甲醇(5.0mL)溶液中的反应混合物于室温下在氢气氛围下搅拌反应过夜。将反应液过滤，浓缩滤液，浓缩物经制备型HPLC纯化，得到目标产物。(R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine-4- The reaction mixture of oxy)quinazolin-4-amine (100.0 mg, 0.19 mmol) and Pd/C (20.0 mg) in methanol (5.0 mL) was stirred at room temperature under a hydrogen atmosphere overnight. The reaction solution was filtered, the filtrate was concentrated, and the concentrate was purified by preparative HPLC to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝476.3. LC-MS: (ESI, m/z): [M+H] + = 476.3.
1H NMR(400MHz,DMSO-d 6)δ7.91(d,J＝7.9Hz,1H),7.78(s,1H),7.04(s,1H),6.88(s,1H),6.85(s,1H),6.69(s,1H),5.66-5.46(m,3H),4.54-5.48(m,1H),3.87(s,3H),3.01-2.93(m,2H),2.64-2.53(m,2H),2.35(s,3H),1.93-1.89(m,2H),1.58-1.44(m,5H). 1 H NMR (400MHz, DMSO-d 6 )δ7.91(d, J=7.9Hz, 1H), 7.78(s, 1H), 7.04(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.69(s, 1H), 5.66-5.46(m, 3H), 4.54-5.48(m, 1H), 3.87(s, 3H), 3.01-2.93(m, 2H), 2.64-2.53(m, 2H), 2.35(s, 3H), 1.93-1.89(m, 2H), 1.58-1.44(m, 5H).
中间体11：4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯Intermediate 11: Pentafluorophenyl 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate
步骤1：4-((2-羧基乙基)氨基)苯甲酸的制备Step 1: Preparation of 4-((2-carboxyethyl)amino)benzoic acid
Figure PCTCN2022088560-appb-000587
Figure PCTCN2022088560-appb-000587
将丙烯酸(23.62g,328.1mmol)加入4-氨基苯甲酸(15.0g,109.4mmol)的AcOH/H 2O(40ml/200mL)溶液中，110℃搅拌12小时，反应液冷却，过滤，得到目标产物4-((2-羧乙基)氨基)苯甲酸。 Acrylic acid (23.62 g, 328.1 mmol) was added to the AcOH/H 2 O (40 ml/200 mL) solution of 4-aminobenzoic acid (15.0 g, 109.4 mmol), stirred at 110° C. for 12 hours, the reaction solution was cooled and filtered to obtain the target The product 4-((2-carboxyethyl)amino)benzoic acid.
LC-MS:(ESI,m/z):[M+H] +＝210.0. LC-MS: (ESI, m/z): [M+H] + = 210.0.
步骤2：4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸的制备Step 2: Preparation of 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid
Figure PCTCN2022088560-appb-000588
Figure PCTCN2022088560-appb-000588
将尿素(114.83g,1913.8mmol)加入到4-((2-羧乙基)氨基)苯甲酸(20.0g,95.69mmol)的AcOH(240mL)溶液中，110℃搅拌24h，反应液冷却后，加入HCl溶液，调节pH值至1-2，析出固体，过滤，得到目标产物4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸。Urea (114.83 g, 1913.8 mmol) was added to a solution of 4-((2-carboxyethyl)amino)benzoic acid (20.0 g, 95.69 mmol) in AcOH (240 mL), and stirred at 110° C. for 24 h. After the reaction solution was cooled, HCl solution was added, the pH value was adjusted to 1-2, a solid was precipitated and filtered to obtain the target product 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid.
LC-MS:(ESI,m/z):[M+H] +＝233.1. LC-MS: (ESI, m/z): [M+H] + = 233.1.
步骤3：4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯的制备Step 3: Preparation of Pentafluorophenyl 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate
Figure PCTCN2022088560-appb-000589
Figure PCTCN2022088560-appb-000589
五氟苯酚(12.97g,70.51mmol)和DCC(14.52g,70.51mmol)加入到4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸(15.0g,64.1mmol)的DMF(200mL)溶液中，室温搅拌过夜，用乙酸乙酯(100mL×3)萃取，饱和食盐水(300mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝3:7)纯化得到目标产物4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯。Pentafluorophenol (12.97 g, 70.51 mmol) and DCC (14.52 g, 70.51 mmol) were added to 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid (15.0 g, 64.1 mmol) in DMF (200 mL) solution, stirred overnight at room temperature, extracted with ethyl acetate (100 mL×3), washed the organic phase with saturated brine (300 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was used Column chromatography (EA:PE=3:7) was used to obtain the target product 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester.
1H NMR(400MHz,DMSO-d 6)δ10.59(s,1H),8.20(d,J＝8.7Hz,2H),7.64(d,J＝8.7Hz,2H),3.94(t,J＝6.6Hz,2H),2.76(t,J＝6.6Hz,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.59 (s, 1H), 8.20 (d, J=8.7Hz, 2H), 7.64 (d, J=8.7Hz, 2H), 3.94 (t, J= 6.6Hz, 2H), 2.76(t, J=6.6Hz, 2H).
中间体12:(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯Intermediate 12: tert-butyl (R)-(3-(1-aminoethyl)-5-(trifluoromethyl)phenyl)carbamate
步骤1：1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-酮的制备Step 1: Preparation of 1-(3-nitro-5-(trifluoromethyl)phenyl)ethan-1-one
Figure PCTCN2022088560-appb-000590
Figure PCTCN2022088560-appb-000590
将1-溴-3-硝基-5-(三氟甲基)苯(50.0g,185.1mmol)，Pd(PPh 3) 2Cl 2(12.9g,18.5mmol)，TEA(37.4g,370.2mmol)和三丁基(1-乙氧基乙烯基)锡烷(86.6g,240.6mmol)在二氧六环(300mL)中的反应液在80℃搅拌16h。反应液中加入水(900mL)淬灭反应，用EA(500mL×3)，合并有机相并用饱和食盐水洗涤，经无水Na 2SO 4干燥，减压浓缩。残余物在6N HCl(200mL)和THF(200mL)的混合溶液中搅拌30min，然后加入水(500mL)，EA(500mL×2)，合并有机相，饱和食盐水洗涤经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(EA:PE＝0～1:9)纯化得到1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-酮。 1-Bromo-3-nitro-5-(trifluoromethyl)benzene (50.0 g, 185.1 mmol), Pd(PPh 3 ) 2 Cl 2 (12.9 g, 18.5 mmol), TEA (37.4 g, 370.2 mmol) ) and tributyl(1-ethoxyvinyl)stannane (86.6 g, 240.6 mmol) in dioxane (300 mL) was stirred at 80 °C for 16 h. Water (900 mL) was added to the reaction solution to quench the reaction, and the organic phases were combined with EA (500 mL×3) and washed with saturated brine, dried over anhydrous Na 2 SO 4 and concentrated under reduced pressure. The residue was stirred in a mixed solution of 6N HCl (200 mL) and THF (200 mL) for 30 min, then water (500 mL), EA (500 mL×2) were added, the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. , concentrated under reduced pressure. The crude product was purified by column chromatography (EA:PE=0-1:9) to obtain 1-(3-nitro-5-(trifluoromethyl)phenyl)ethan-1-one.
1H NMR(400MHz,CDCl 3)δ8.95(s,1H),8.69(s,1H),8.53(s,1H),2.75(s,3H). 1 H NMR (400MHz, CDCl 3 ) δ 8.95(s,1H), 8.69(s,1H), 8.53(s,1H), 2.75(s,3H).
步骤2：1-(3-氨基-5-(三氟甲基)苯基)乙烷-1-酮的制备Step 2: Preparation of 1-(3-amino-5-(trifluoromethyl)phenyl)ethan-1-one
Figure PCTCN2022088560-appb-000591
Figure PCTCN2022088560-appb-000591
将1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-酮(1.5g,6.4mmol)和Pd/C(400mg)在THF(30mL)中的混合物在60℃搅拌16h。反应液过滤，滤液减压浓缩得到1-(3-氨基-5-(三氟甲基)苯基)乙烷-1-酮。所得产物直接用于下一步反应。A mixture of 1-(3-nitro-5-(trifluoromethyl)phenyl)ethan-1-one (1.5 g, 6.4 mmol) and Pd/C (400 mg) in THF (30 mL) was added at 60 °C stirred for 16h. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure to obtain 1-(3-amino-5-(trifluoromethyl)phenyl)ethan-1-one. The obtained product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝203.0. LC-MS: (ESI, m/z): [M+H] + = 203.0.
步骤3：(3-乙酰基-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 3: Preparation of tert-butyl (3-acetyl-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000592
Figure PCTCN2022088560-appb-000592
将1-(3-氨基-5-(三氟甲基)苯基)乙烷-1-酮(1.1g,5.4mmol)和(Boc) 2O(5.9g,27.0mmol)在二氧六环(20mL)中的混合物在80℃搅拌16h。反应液直接减压浓缩，所得粗产物经层析柱(EA:PE＝0～3:17)纯化得到(3-乙酰基-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 Mix 1-(3-amino-5-(trifluoromethyl)phenyl)ethan-1-one (1.1 g, 5.4 mmol) and (Boc)2O (5.9 g , 27.0 mmol) in dioxane The mixture in (20 mL) was stirred at 80 °C for 16 h. The reaction solution was directly concentrated under reduced pressure, and the obtained crude product was purified by column chromatography (EA:PE=0～3:17) to obtain tert-butyl (3-acetyl-5-(trifluoromethyl)phenyl)carbamate.
LC-MS:(ESI,m/z):[M+H] +＝303.0. LC-MS: (ESI, m/z): [M+H] + = 303.0.
1H NMR(400MHz,DMSO-d 6)δ8.26(s,1H),8.18(d,J＝6.5Hz,1H),8.05(s,1H),2.67(d,J＝11.4Hz,3H),1.41(d,J＝11.7Hz,9H). 1 H NMR (400MHz, DMSO-d 6 ) δ 8.26(s, 1H), 8.18(d, J=6.5Hz, 1H), 8.05(s, 1H), 2.67(d, J=11.4Hz, 3H) ,1.41(d,J=11.7Hz,9H).
步骤4：(S,E)-(3-(1-((叔-丁基亚硫酰基)亚氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 4: Preparation of tert-butyl (S,E)-(3-(1-((tert-butylsulfinyl)imino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000593
Figure PCTCN2022088560-appb-000593
将(3-乙酰基-5-(三氟甲基)苯基)氨基甲酸叔丁酯(1.0g,3.3mmol)，Ti(OEt) 4(1.8g,6.6mmol)，二乙烯二醇二甲基醚(2.3g,17.5mmol)和(S)-丙烷-2-亚磺酰胺(1.2g,9.9mmol)在THF(10mL)中的混合物在70℃搅拌12h。反应液中加水(50mL)，用EA(30mL×3)萃取，合并有机相，饱和食盐水洗涤经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(EA:PE＝0～1:4)纯化得到(S,E)-(3-(1-((叔-丁基亚硫酰基)亚氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯. (3-Acetyl-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester (1.0 g, 3.3 mmol), Ti(OEt) 4 (1.8 g, 6.6 mmol), diethylene glycol dimethyl A mixture of base ether (2.3 g, 17.5 mmol) and (S)-propane-2-sulfinamide (1.2 g, 9.9 mmol) in THF (10 mL) was stirred at 70 °C for 12 h. Water (50 mL) was added to the reaction solution, extracted with EA (30 mL×3), the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (EA:PE=0～1:4) to obtain (S,E)-(3-(1-((tert-butylsulfinyl)imino)ethyl)-5-( tert-butyl trifluoromethyl)phenyl)carbamate.
LC-MS:(ESI,m/z):[M+H] +＝407.0. LC-MS: (ESI, m/z): [M+H] + = 407.0.
步骤5：(3-((R)-1-(((S)-叔-丁基亚硫酰基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 5: tert-butyl (3-((R)-1-(((S)-tert-butylsulfinyl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate preparation
Figure PCTCN2022088560-appb-000594
Figure PCTCN2022088560-appb-000594
-78℃时，向(S,E)-(3-(1-((叔-丁基亚硫酰基<亚磺酰>)亚氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(1.0g,2.4mmol)的THF(20mL)溶液中加入L-Selectride(1.0mol/L/THF,3.6mL)，反应液在-78℃搅拌50min。反应液中加入水(50mL)淬灭反应，然后用EA(50mL×2)萃取，合并有机相，饱和食盐水洗涤经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(EA:PE＝0～1:1)纯化得到(3-((R)-1-(((S)-叔-丁基亚硫酰基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。-78°C to (S,E)-(3-(1-((tert-butylsulfinyl<sulfinyl>)imino)ethyl)-5-(trifluoromethyl)phenyl ) To the solution of tert-butyl carbamate (1.0 g, 2.4 mmol) in THF (20 mL), L-Selectride (1.0 mol/L/THF, 3.6 mL) was added, and the reaction solution was stirred at -78° C. for 50 min. Water (50 mL) was added to the reaction solution to quench the reaction, and then extracted with EA (50 mL×2). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (EA:PE=0～1:1) to obtain (3-((R)-1-(((S)-tert-butylsulfinyl)amino)ethyl)-5- tert-butyl (trifluoromethyl)phenyl)carbamate.
LC-MS:(ESI,m/z):[M+H] +＝409.0. LC-MS: (ESI, m/z): [M+H] + = 409.0.
1H NMR(400MHz,DMSO-d 6)δ9.71(s,1H),7.74(d,J＝5.1Hz,2H),7.39(s,1H),4.15(q,J＝6.7Hz,1H),1.48(s,15H),1.31(d,J＝6.7Hz,3H),1.11(d,J＝2.1Hz,3H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 9.71 (s, 1H), 7.74 (d, J=5.1 Hz, 2H), 7.39 (s, 1H), 4.15 (q, J=6.7 Hz, 1H) ,1.48(s,15H),1.31(d,J=6.7Hz,3H),1.11(d,J=2.1Hz,3H).
步骤6：(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 6: Preparation of tert-butyl (R)-(3-(1-aminoethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000595
Figure PCTCN2022088560-appb-000595
0℃下将(3-((R)-1-(((S)-叔-丁基亚硫酰基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(1.0g,2.4mmol)在1N HCl/EtOAc(20mL)中搅拌3h。反应液经层析柱快速过滤，先用EtOAc冲洗，再用DCM/MeOH(5/1)混合溶剂冲洗，滤液用7N NH 3/MeOH碱化，有机相水洗，经无水Na 2SO 4干燥，过滤，浓缩得到(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 (3-((R)-1-(((S)-tert-butylsulfinyl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester at 0°C (1.0 g, 2.4 mmol) was stirred in 1 N HCl/EtOAc (20 mL) for 3 h. The reaction solution was quickly filtered through a chromatographic column, washed with EtOAc, and then with a mixed solvent of DCM/MeOH (5/1), the filtrate was basified with 7N NH 3 /MeOH, the organic phase was washed with water, and dried over anhydrous Na 2 SO 4 . , filtered and concentrated to give tert-butyl (R)-(3-(1-aminoethyl)-5-(trifluoromethyl)phenyl)carbamate.
LC-MS:(ESI,m/z):[M+H] +＝305.1. LC-MS: (ESI, m/z): [M+H] + = 305.1.
1H NMR(400MHz,DMSO-d 6)δ9.63(s,1H),7.71(s,1H),7.69(s,1H),7.35(s,1H),4.02–3.99(m,1H),1.48(s,9H),1.23(d,J＝6.6Hz,3H). 1 H NMR (400MHz, DMSO-d 6 )δ9.63(s,1H), 7.71(s,1H), 7.69(s,1H), 7.35(s,1H), 4.02–3.99(m,1H), 1.48(s, 9H), 1.23(d, J=6.6Hz, 3H).
中间体13：(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯Intermediate 13: (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000596
Figure PCTCN2022088560-appb-000596
边搅拌边向(1R,4R)-4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(330mg,1.0mmol)的 DMF(5mL)溶液中加入BOP(574mg,1.3mmol)和DBU(380mg,2.5mmol)，搅拌15min后，再加入(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯盐酸盐(396mg,1.3mmol)，反应液在70℃继续搅拌12h。反应液中加水(10mL)淬灭反应，然后用EA(30mL×3)萃取。有机相用无水Na 2SO 4干燥，然后减压浓缩。所得粗品经层析柱(EA:PE＝0～1)纯化得到(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 To (1R,4R)-4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid methyl ester (330 mg, 1.0 mmol) was added with stirring. ) in DMF (5 mL) solution was added BOP (574 mg, 1.3 mmol) and DBU (380 mg, 2.5 mmol), and after stirring for 15 min, (R)-(3-(1-aminoethyl)-5-(trimethylamine) was added. Fluoromethyl)phenyl)carbamate tert-butyl ester hydrochloride (396 mg, 1.3 mmol), the reaction solution was further stirred at 70° C. for 12 h. Water (10 mL) was added to the reaction solution to quench the reaction, and then extracted with EA (30 mL×3). The organic phase was dried over anhydrous Na 2 SO 4 and then concentrated under reduced pressure. The obtained crude product was purified by chromatography column (EA:PE=0~1) to obtain (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)- 5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝617.4. LC-MS: (ESI, m/z): [M+H] + = 617.4.
1H NMR(400MHz,DMSO-d 6)δ9.69(s,1H),8.12(s,1H),7.77(d,J＝25.2Hz,2H),7.41(s,1H),7.01(s,1H),5.71–5.55(m,1H),3.90(s,3H),3.62(s,3H),2.96(d,J＝11.8Hz,1H),2.39(d,J＝10.4Hz,4H),2.06(d,J＝12.0Hz,2H),1.89(d,J＝14.0Hz,2H),1.64–1.50(m,7H),1.46(s,9H). 1 H NMR (400MHz, DMSO-d 6 ) δ 9.69(s, 1H), 8.12(s, 1H), 7.77(d, J=25.2Hz, 2H), 7.41(s, 1H), 7.01(s, 1H), 5.71–5.55(m, 1H), 3.90(s, 3H), 3.62(s, 3H), 2.96(d, J=11.8Hz, 1H), 2.39(d, J=10.4Hz, 4H), 2.06(d,J＝12.0Hz,2H),1.89(d,J＝14.0Hz,2H),1.64-1.50(m,7H),1.46(s,9H).
中间体14：(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸Intermediate 14: (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000597
Figure PCTCN2022088560-appb-000597
向(1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(250mg,0.4mmol)的THF/H 2O(10mL/5mL)溶液中加入LiOH.H 2O(48mg,1.2mmol)，反应液在40℃搅拌过夜。反应液用10％柠檬酸调节至pH为，然后用EtOAc(30mL×3)萃取，合并有机相，用饱和食盐水洗涤，减压浓缩得到(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 To (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (250 mg, 0.4 mmol) in THF/H 2 O (10 mL/5 mL) was added LiOH.H 2 O (48 mg, 1.2 mmol), the reaction was stirred at 40° C. overnight. The reaction solution was adjusted to pH 0 with 10% citric acid, then extracted with EtOAc (30 mL×3), the organic phases were combined, washed with saturated brine, and concentrated under reduced pressure to obtain (1R,4R)-4-(4-((( R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝603.1. LC-MS: (ESI, m/z): [M+H] + = 603.1.
1H NMR(400MHz,DMSO-d 6)δ9.67(s,1H),8.20(d,J＝7.4Hz,1H),8.07(s,1H),7.77(d,J＝24.0Hz,2H),7.41(s,1H),7.00(s,1H),5.68–5.52(m,1H),3.89(s,3H),2.95(d,J＝11.3Hz,1H),2.40–2.23(m,4H),2.06(d,J＝12.0Hz,2H),1.88(d,J＝12.0Hz,2H),1.67–1.41(m,16H). 1 H NMR (400MHz, DMSO-d 6 ) δ 9.67(s, 1H), 8.20(d, J=7.4Hz, 1H), 8.07(s, 1H), 7.77(d, J=24.0Hz, 2H) ,7.41(s,1H),7.00(s,1H),5.68–5.52(m,1H),3.89(s,3H),2.95(d,J=11.3Hz,1H),2.40–2.23(m,4H) ), 2.06(d, J＝12.0Hz, 2H), 1.88(d, J＝12.0Hz, 2H), 1.67–1.41(m, 16H).
中间体15：(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸Intermediate 15: (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl) )ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid
步骤1：(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 1: (1R,4R)-4-(7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl) Preparation of methyl ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000598
Figure PCTCN2022088560-appb-000598
边搅拌边向(1R,4R)-4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(500mg,1.52mmol)的DMF(10mL)溶液中加入BOP(871mg,1.97mmol)和DBU(577mg,3.80mmol)，继续搅拌15min后，再加入(R)-1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-胺(461mg,1.97mmol)。然后反应液再70℃搅拌过夜。反应液中加水(50mL)，用EA(50mL×3)萃取。合并有机相，用饱和食盐水(100mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(EA:PE＝0～1)纯化得到(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯。 To (1R,4R)-4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (500 mg, 1.52 mmol) was added with stirring. ) in DMF (10 mL) solution was added BOP (871 mg, 1.97 mmol) and DBU (577 mg, 3.80 mmol), and after stirring for 15 min, (R)-1-(3-nitro-5-(trifluoromethane) was added yl)phenyl)ethane-1-amine (461 mg, 1.97 mmol). The reaction solution was then stirred at 70°C overnight. Water (50 mL) was added to the reaction solution, followed by extraction with EA (50 mL×3). The organic phases were combined, washed with saturated brine (100 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～1) to obtain (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro) methyl-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝547.1. LC-MS: (ESI, m/z): [M+H] + = 547.1.
1H NMR(400MHz,DMSO-d 6)δ8.62(s,1H),8.34(d,J＝6.0Hz,3H),8.04(s,1H),7.01(s,1H),5.68(p,J＝6.9Hz,1H),3.89(s,3H),3.64(s,3H),2.94(t,J＝11.4Hz,1H),2.48–2.37(m,1H),2.34(s,3H),2.08(d,J＝12.0Hz,2H),1.97–1.86(m,2H),1.69(d,J＝7.1Hz,3H),1.65–1.47(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 8.62(s, 1H), 8.34(d, J=6.0Hz, 3H), 8.04(s, 1H), 7.01(s, 1H), 5.68(p, J=6.9Hz, 1H), 3.89(s, 3H), 3.64(s, 3H), 2.94(t, J=11.4Hz, 1H), 2.48–2.37(m, 1H), 2.34(s, 3H), 2.08(d,J＝12.0Hz,2H),1.97-1.86(m,2H),1.69(d,J＝7.1Hz,3H),1.65-1.47(m,4H).
步骤2：(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸的制备Step 2: (1R,4R)-4-(7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl) Preparation of ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000599
Figure PCTCN2022088560-appb-000599
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯(300mg,0.55mmol)的THF/H 2O(15mL,1:2)溶液中加入LiOH.H 2O(240mg,8.0mmol)。然后反应液再50℃搅拌过夜。反应液中加入水(50mL)淬灭反应，用EA(50mL×3)萃取。合并有机相，用饱和食盐水(100mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩得到(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸。 To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (300 mg, 0.55 mmol) in THF/H 2 O (15 mL, 1:2) was added LiOH.H 2 O (240 mg) , 8.0 mmol). The reaction solution was then stirred at 50°C overnight. Water (50 mL) was added to the reaction solution to quench the reaction, and extracted with EA (50 mL×3). The organic phases were combined, washed with saturated brine (100 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure to obtain (1R,4R)-4-(7-methoxy-2-methyl-4-( ((R)-1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝533.3. LC-MS: (ESI, m/z): [M+H] + = 533.3.
1H NMR(400MHz,DMSO-d 6)δ12.09(s,1H),8.89(s,1H),8.63(s,1H),8.36(d,J＝10.6Hz,2H),8.14(s,1H),7.02(s,1H),5.89–5.64(m,1H),3.92(s,3H),2.95(t,J＝11.6Hz,1H),2.41(s,3H),2.37–2.26(m,1H),2.08(d,J＝10.7Hz,2H),1.96–1.85(m,2H),1.72(d,J＝7.1Hz,3H),1.68–1.44(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 12.09(s, 1H), 8.89(s, 1H), 8.63(s, 1H), 8.36(d, J=10.6Hz, 2H), 8.14(s, 1H), 7.02(s, 1H), 5.89-5.64(m, 1H), 3.92(s, 3H), 2.95(t, J=11.6Hz, 1H), 2.41(s, 3H), 2.37-2.26(m ,1H),2.08(d,J＝10.7Hz,2H),1.96-1.85(m,2H),1.72(d,J＝7.1Hz,3H),1.68-1.44(m,4H).
中间体16：(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸Intermediate 16: (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carboxylic acid
步骤1：1-(1,3-二羰基异二氢吲哚-2-基)4-甲基(1R,4R)-环己烷-1,4-二羧酸酯的制备Step 1: Preparation of 1-(1,3-Dicarbonylisoindol-2-yl)4-methyl(1R,4R)-cyclohexane-1,4-dicarboxylate
Figure PCTCN2022088560-appb-000600
Figure PCTCN2022088560-appb-000600
向(1R,4R)-4-(甲氧羰基)环己烷-1-羧酸(20g,107.4mmol)和2-羟基异二氢吲哚-1,3-二酮(20g,107.4mmol)的DCM(300mL)溶液中加入EDCI(34.7g,118.2mmol)和DMAP(1.3g,10.7mmol)。然后反应液在室温搅拌2h。反应液中加入食盐水和DCM。分离有机层，用无水Na 2SO 4干燥，过滤，减压浓缩。粗品经层析柱(DCM)纯化得到1-(1,3-二羰基异二氢吲哚-2-基)4-甲基(1R,4R)-环己烷-1,4-二羧酸酯。 To (1R,4R)-4-(methoxycarbonyl)cyclohexane-1-carboxylic acid (20 g, 107.4 mmol) and 2-hydroxyisoindoline-1,3-dione (20 g, 107.4 mmol) To a solution of DCM (300 mL) was added EDCI (34.7 g, 118.2 mmol) and DMAP (1.3 g, 10.7 mmol). The reaction solution was then stirred at room temperature for 2 h. Brine and DCM were added to the reaction solution. The organic layer was separated, dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (DCM) to give 1-(1,3-dicarbonylisoindol-2-yl)4-methyl(1R,4R)-cyclohexane-1,4-dicarboxylic acid ester.
LC-MS:(ESI,m/z):[M+Na] +＝354.1. LC-MS: (ESI, m/z): [M+Na] + = 354.1.
步骤2：2-氨基-5-碘-4-甲氧基苯甲腈的制备Step 2: Preparation of 2-amino-5-iodo-4-methoxybenzonitrile
Figure PCTCN2022088560-appb-000601
Figure PCTCN2022088560-appb-000601
向2-氨基-4-甲氧基苯甲腈(86.3g,582mmol)的DMF(1000mL)溶液中加入NIS(133g,613mmol)。然后反应液在室温搅拌2h。反应液中加入食盐水和DCM。分离有机层，经无水Na 2SO 4干燥过滤，减压浓缩得到2-氨基-5-碘-4-甲氧基苯甲腈。 To a solution of 2-amino-4-methoxybenzonitrile (86.3 g, 582 mmol) in DMF (1000 mL) was added NIS (133 g, 613 mmol). The reaction solution was then stirred at room temperature for 2 h. Brine and DCM were added to the reaction solution. The organic layer was separated, dried over anhydrous Na2SO4 , filtered, and concentrated under reduced pressure to give 2-amino-5-iodo- 4 -methoxybenzonitrile.
LC-MS:(ESI,m/z):[M+Na] +＝296.9. LC-MS: (ESI, m/z): [M+Na] + = 296.9.
步骤3：N-(2-氰基-4-碘-5-甲氧苯基)乙酰胺的制备Step 3: Preparation of N-(2-cyano-4-iodo-5-methoxyphenyl)acetamide
Figure PCTCN2022088560-appb-000602
Figure PCTCN2022088560-appb-000602
向2-氨基-5-碘-4-甲氧基苯甲腈(160g,580mmol)的HOAc(1600mL)溶液中加入Ac 2O(71.3g,700mmol)。然后反应液在室温搅拌过夜。反应液过滤然后浓缩得到N-(2-氰基-4-碘-5-甲氧苯基)乙酰胺。 To a solution of 2-amino-5-iodo-4-methoxybenzonitrile (160 g, 580 mmol) in HOAc (1600 mL) was added Ac2O (71.3 g, 700 mmol). The reaction was then stirred at room temperature overnight. The reaction solution was filtered and concentrated to obtain N-(2-cyano-4-iodo-5-methoxyphenyl)acetamide.
LC-MS:(ESI,m/z):[M+H] +＝317.0. LC-MS: (ESI, m/z): [M+H] + = 317.0.
步骤4：(1R,4R)-4-(4-乙酰氨基-5-氰基-2-甲氧苯基)环己烷-1-羧酸甲酯的制备Step 4: Preparation of methyl (1R,4R)-4-(4-acetamido-5-cyano-2-methoxyphenyl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000603
Figure PCTCN2022088560-appb-000603
向N-(2-氰基-4-碘-5-甲氧苯基)乙酰胺(15.0g,47.45mmol)，1-(1,3-二羰基异二氢吲哚-2-基)4-甲基(1R,4R)-环己烷-1,4-二羧酸酯(31.40g,94.90mmol)和Hantzsch-ester(24.00g,94.90mmol)的DMA(237mL,0.2M)溶液中加NiBr 2(dtbpy)(2.31g,4.75mmol)。反应液用N 2吹5分钟并两个Kessil PR160-purple LED lamps(30W High Luminous DEX 2100 LED,λmax＝390nm)照射16h。反应温度控制在30-40℃。反应结束后，反应液倒入水(1L)中，然后用EtOAc(150mLx3)萃取。合并有机相并用饱和食盐水(400mLx3)洗涤，经无水Na 2SO 4干燥，减压浓缩。所得粗品经层析柱(MeOH:DCM＝1:99)纯化。收集含有产物的洗脱液浓缩值80mL，过滤，滤液浓缩得到顺反比列为1:1的混合物，滤饼为顺反比列为15:1的混合物。将顺反比列为15:1的混合物溶解在DMA(85mL)中，然后加入0.5M K 2CO 3水溶液(200mL)，所得混合物室温搅拌2小时，过滤得到顺反比列为20:1的混合物，将此混合物用乙腈(180mL)进行重结晶得到目标产物(顺反比例为97:2) To N-(2-cyano-4-iodo-5-methoxyphenyl)acetamide (15.0 g, 47.45 mmol), 1-(1,3-dicarbonylisoindol-2-yl)4 -Methyl(1R,4R)-cyclohexane-1,4-dicarboxylate (31.40 g, 94.90 mmol) and Hantzsch-ester (24.00 g, 94.90 mmol) in DMA (237 mL, 0.2 M) were added NiBr2 (dtbpy) (2.31 g, 4.75 mmol). The reaction solution was purged with N 2 for 5 minutes and irradiated with two Kessil PR160-purple LED lamps (30W High Luminous DEX 2100 LED, λmax=390nm) for 16h. The reaction temperature was controlled at 30-40°C. After the reaction, the reaction solution was poured into water (1 L), and then extracted with EtOAc (150 mL×3). The organic phases were combined and washed with saturated brine (400 mL×3), dried over anhydrous Na 2 SO 4 , and concentrated under reduced pressure. The obtained crude product was purified by chromatography column (MeOH:DCM=1:99). The eluate containing the product was collected with a concentration of 80 mL, filtered, and the filtrate was concentrated to obtain a mixture with a cis-trans ratio of 1:1, and the filter cake was a mixture with a cis-trans ratio of 15:1. The mixture with a cis-trans ratio of 15:1 was dissolved in DMA (85 mL), then a 0.5M aqueous K 2 CO 3 solution (200 mL) was added, the resulting mixture was stirred at room temperature for 2 hours, and filtered to obtain a cis-trans ratio of 20: 1. The mixture was recrystallized from acetonitrile (180 mL) to obtain the desired product (cis-trans ratio 97:2)
LC-MS:(ESI,m/z):[M+H] +＝331.1. LC-MS: (ESI, m/z): [M+H] + = 331.1.
1H NMR(400MHz,CDCl 3)δ8.04(s,1H),7.55(s,1H),7.29(s,1H),3.89(s,3H),3.69(s,3H),2.90-2.84(m,1H),2.35-2.26(m,1H),2.25(s,3H),2.11-2.08(m,2H),1.92-1.89(m,2H),1.63-1.56(m,2H),1.39-1.33(m,2H). 1 H NMR (400MHz, CDCl 3 )δ8.04(s,1H), 7.55(s,1H), 7.29(s,1H), 3.89(s,3H), 3.69(s,3H), 2.90-2.84( m,1H),2.35-2.26(m,1H),2.25(s,3H),2.11-2.08(m,2H),1.92-1.89(m,2H),1.63-1.56(m,2H),1.39- 1.33(m,2H).
步骤5：(1R,4R)-4-(7-甲氧基-2-甲基-4-羰基-3,4-二氢喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 5: (1R,4R)-4-(7-Methoxy-2-methyl-4-carbonyl-3,4-dihydroquinazolin-6-yl)cyclohexane-1-carboxylate methyl Preparation of esters
Figure PCTCN2022088560-appb-000604
Figure PCTCN2022088560-appb-000604
将(1R,4R)-4-(4-乙酰氨基-5-氰基-2-甲氧苯基)环己烷-1-羧酸甲酯(3g,9.08mmol)加到i-PrOH(80mL)中，,然后室温下通HCl气体1h。将反应液过滤，干燥得到(1R,4R)-4-(7-甲氧基-2-甲基-4-羰基-3,4-二氢喹唑啉-6-基)环己烷-1-羧酸甲酯。Methyl (1R,4R)-4-(4-acetamido-5-cyano-2-methoxyphenyl)cyclohexane-1-carboxylate (3 g, 9.08 mmol) was added to i-PrOH (80 mL) ), and then passed HCl gas for 1 h at room temperature. The reaction solution was filtered and dried to obtain (1R,4R)-4-(7-methoxy-2-methyl-4-carbonyl-3,4-dihydroquinazolin-6-yl)cyclohexane-1 - Methyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝331.1. LC-MS: (ESI, m/z): [M+H] + = 331.1.
1H NMR(400MHz,DMSO-d 6)δ7.87(s,1H),7.23(s,1H),3.95(s,3H),3.61(s,3H),2.98-2.87(m,1H),2.58(s,3H),2.47-2.39(m,1H),2.06-1.98(m,2H),1.88-1.80(m,2H),1.59-1.42(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ7.87(s,1H), 7.23(s,1H), 3.95(s,3H), 3.61(s,3H), 2.98-2.87(m,1H), 2.58(s, 3H), 2.47-2.39(m, 1H), 2.06-1.98(m, 2H), 1.88-1.80(m, 2H), 1.59-1.42(m, 4H).
步骤6：(R,Z)-N-(1-(4-溴噻吩-2-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 6: Preparation of (R,Z)-N-(1-(4-bromothiophen-2-yl)ethylene)-2-methylpropane-2-sulfinamide
Figure PCTCN2022088560-appb-000605
Figure PCTCN2022088560-appb-000605
将1-(4-溴噻吩-2-基)乙烷-1-酮(10.0g,48.80mmol)，(R)-2-甲基丙烷-2-亚磺酰胺(8.90g,73.20mmol)和Ti(OEt) 4(27.8g,122.00mmol)在THF(70mL)中的反应液在80℃搅拌3h。反应液中加水(200mL)淬灭，然后用EA(100mLx3)萃取。合并有机相，经无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经层析柱(DCM:MeOH＝100:1)纯化得到(R,Z)-N-(1-(4-溴噻吩-2-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺。 1-(4-Bromothiophen-2-yl)ethan-1-one (10.0 g, 48.80 mmol), (R)-2-methylpropane-2-sulfinamide (8.90 g, 73.20 mmol) and The reaction of Ti(OEt) 4 (27.8 g, 122.00 mmol) in THF (70 mL) was stirred at 80 °C for 3 h. The reaction solution was quenched by adding water (200 mL), and then extracted with EA (100 mL×3). The organic phases were combined, dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by column chromatography (DCM:MeOH=100:1) to give (R,Z)-N-(1-(4-bromothiophen-2-yl)ethylene)-2-methylpropane-2 - Sulfenamide.
1H NMR(400MHz,DMSO-d 6)δ7.96(d,J＝1.2Hz,1H),7.85(d,J＝1.2Hz,1H),2.68(s,3H),1.19(s,9H). 1 H NMR (400MHz, DMSO-d 6 )δ7.96(d,J=1.2Hz,1H),7.85(d,J=1.2Hz,1H),2.68(s,3H),1.19(s,9H) .
步骤7：(R)-N-((R)-1-(4-溴噻吩-2-基)乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 7: Preparation of (R)-N-((R)-1-(4-bromothiophen-2-yl)ethyl)-2-methylpropane-2-sulfinamide
Figure PCTCN2022088560-appb-000606
Figure PCTCN2022088560-appb-000606
向(R,Z)-N-(1-(4-溴噻吩-2-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺(7.0g,22.7mmol)的THF(10mL)溶液中加9-BBN/THF(0.5M,200mL)。反应液在25℃搅拌0.5h。反应液中加MeOH(10mL)淬灭反应，然后加入水(100mL)，再用EA(100mLx3)萃取。合并有机相用无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经层析柱(DCM:MeOH＝100:1)纯化得到(R)-N-((R)-1-(4-溴噻吩-2-基)乙基)-2-甲基丙烷-2-亚磺酰胺。 To (R,Z)-N-(1-(4-bromothiophen-2-yl)ethylene)-2-methylpropane-2-sulfenamide (7.0 g, 22.7 mmol) in THF (10 mL) To the solution was added 9-BBN/THF (0.5M, 200 mL). The reaction solution was stirred at 25°C for 0.5h. MeOH (10 mL) was added to the reaction solution to quench the reaction, and then water (100 mL) was added, followed by extraction with EA (100 mL×3). The combined organic phases were dried over anhydrous Na2SO4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by column chromatography (DCM:MeOH=100:1) to give (R)-N-((R)-1-(4-bromothiophen-2-yl)ethyl)-2-methylpropane- 2-Sulfinamide.
1H NMR(400MHz,DMSO-d 6)δ7.54(d,J＝1.2Hz,1H),7.08(s,1H),5.93(d,J＝7.2Hz,1H),4.64-4.58(m,1H),1.48(d,J＝6.8Hz,3H),1.12(s,9H). 1 H NMR (400MHz, DMSO-d 6 ) δ 7.54 (d, J=1.2Hz, 1H), 7.08 (s, 1H), 5.93 (d, J=7.2Hz, 1H), 4.64-4.58 (m, 1H), 1.48(d, J=6.8Hz, 3H), 1.12(s, 9H).
步骤8：(R)-1-(4-溴噻吩-2-基)乙烷-1-胺盐酸盐的制备Step 8: Preparation of (R)-1-(4-bromothiophen-2-yl)ethane-1-amine hydrochloride
Figure PCTCN2022088560-appb-000607
Figure PCTCN2022088560-appb-000607
向(R)-N-((R)-1-(4-溴噻吩-2-基)乙基)-2-甲基丙烷-2-亚磺酰胺(6.0g,19.34mmol)的1,4-二氧六环(60mL)溶液中加HCl(12M,454mmol)。然后反应液在25℃搅拌2h。反应液直接浓缩。所得粗品在MTBE(100mL)溶液中搅拌，过滤，干燥得到(R)-1-(4-溴噻吩-2-基)乙烷-1-胺盐酸盐。To (R)-N-((R)-1-(4-bromothiophen-2-yl)ethyl)-2-methylpropane-2-sulfinamide (6.0 g, 19.34 mmol) in 1,4 - To a solution of dioxane (60 mL) was added HCl (12 M, 454 mmol). The reaction solution was then stirred at 25°C for 2h. The reaction solution was directly concentrated. The resulting crude product was stirred in MTBE (100 mL) solution, filtered and dried to give (R)-1-(4-bromothiophen-2-yl)ethane-1-amine hydrochloride.
1H NMR(400MHz,DMSO-d 6)δ8.62(s,3H),7.71(s,1H),7.32(s,1H),4.71-4.67(m,1H),1.57(d,J＝6.8Hz,3H). 1 H NMR (400MHz, DMSO-d 6 )δ8.62(s, 3H), 7.71(s, 1H), 7.32(s, 1H), 4.71-4.67(m, 1H), 1.57(d, J=6.8 Hz, 3H).
步骤9：(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 9: (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazole Preparation of olin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000608
Figure PCTCN2022088560-appb-000608
室温时向(1R,4R)-4-(7-甲氧基-2-甲基-4-羰基-3,4-二氢喹唑啉-6-基)环己烷-1-羧酸甲酯(3.00g,9.07mmol)和BOP(5.21g,11.79mmol)的DMF(35mL)溶液中加DBU(3.45g,22.67mmol)，搅拌15分钟后，滴加(R)-1-(4-溴噻吩-2-基)乙烷-1-胺盐酸盐(2.86g,11.79mmol)的DMF(35mL)溶液，然后反应液先在室温搅拌20分钟，再升温至70℃搅拌8小时。反应液经反相柱纯化得到(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。To (1R,4R)-4-(7-methoxy-2-methyl-4-carbonyl-3,4-dihydroquinazolin-6-yl)cyclohexane-1-carboxylate methyl at room temperature To a solution of ester (3.00 g, 9.07 mmol) and BOP (5.21 g, 11.79 mmol) in DMF (35 mL) was added DBU (3.45 g, 22.67 mmol), and after stirring for 15 minutes, (R)-1-(4- Bromothiophen-2-yl)ethane-1-amine hydrochloride (2.86 g, 11.79 mmol) in DMF (35 mL), the reaction solution was stirred at room temperature for 20 minutes, then heated to 70°C and stirred for 8 hours. The reaction solution was purified by reverse phase column to obtain (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝518.0,520.0. LC-MS: (ESI, m/z): [M+H] + = 518.0, 520.0.
步骤10：(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 10: (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazole Preparation of olin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000609
Figure PCTCN2022088560-appb-000609
向(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(2.00g,3.86mmol)的THF/H 2O(20.0mL/20.0mL)溶液中加LiOH(0.81g,19.30mmol)。反应液在25℃搅拌16h。反应液用2N HCl溶液酸化，有沉淀生成。过滤，滤饼真空干燥得到(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 To (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- To a solution of methyl 6-yl)cyclohexane-1-carboxylate (2.00 g, 3.86 mmol) in THF/ H2O (20.0 mL/20.0 mL) was added LiOH (0.81 g, 19.30 mmol). The reaction solution was stirred at 25°C for 16h. The reaction solution was acidified with 2N HCl solution, and a precipitate formed. Filtration and vacuum drying of the filter cake gave (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝504.0,506.0. LC-MS: (ESI, m/z): [M+H] + = 504.0, 506.0.
中间体17：4-(2,6-二氧代基哌啶-3-基)苯甲酸五氟苯酯Intermediate 17: Pentafluorophenyl 4-(2,6-dioxopiperidin-3-yl)benzoate
步骤1：4-(4-氰基-1-甲氧基-1-氧丁烷-2-基)苯甲酸甲酯的制备Step 1: Preparation of methyl 4-(4-cyano-1-methoxy-1-oxobutan-2-yl)benzoate
Figure PCTCN2022088560-appb-000610
Figure PCTCN2022088560-appb-000610
将苄基三甲基氢氧化铵(6.03g,36.057mmol)和丙烯腈(5.727g,79.32mmol)加入4-(2-甲氧基-2-氧乙烷)苯甲酸甲酯(15.0g,72.12mmol)的甲苯溶液(200mL)中，30℃搅拌16h，，用乙酸乙酯(100mL×5)提取，饱和食盐水(500mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝3:7)纯化得到目标产物4-(4-氰基-1-甲氧基-1-氧丁烷-2-基)苯甲酸甲酯。Benzyltrimethylammonium hydroxide (6.03 g, 36.057 mmol) and acrylonitrile (5.727 g, 79.32 mmol) were added to methyl 4-(2-methoxy-2-oxoethane)benzoate (15.0 g, 72.12 mmol) in toluene solution (200 mL), stirred at 30°C for 16 h, extracted with ethyl acetate (100 mL×5), washed the organic phase with saturated brine (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure , the crude product was purified by column chromatography (EA:PE=3:7) to obtain the target product, methyl 4-(4-cyano-1-methoxy-1-oxobutan-2-yl)benzoate.
1H NMR(400MHz,DMSO-d 6)δ7.95(d,J＝4.0Hz,2H),7.46(d,J＝6.0Hz,2H),3.90-3.80(m,4H),3.62(s,3H),2.48-2.38(m,2H),2.36-2.26(m,1H),2.10-1.96(m,1H). 1 H NMR (400MHz, DMSO-d 6 ) δ 7.95(d, J=4.0Hz, 2H), 7.46(d, J=6.0Hz, 2H), 3.90-3.80(m, 4H), 3.62(s, 3H), 2.48-2.38(m, 2H), 2.36-2.26(m, 1H), 2.10-1.96(m, 1H).
步骤2：4-(2,6-二氧哌啶-3-基)苯甲酸的制备Step 2: Preparation of 4-(2,6-Dioxypiperidin-3-yl)benzoic acid
Figure PCTCN2022088560-appb-000611
Figure PCTCN2022088560-appb-000611
将4-(4-氰基-1-甲氧基-1-氧丁烷-2-基)苯甲酸甲酯(8.5g,32.56mmol)溶解在乙酸(30mL)中，加入硫酸(15mL)，110℃搅拌12h，用二氯甲烷/甲醇(10/1,150ml×3)提取，饱和食盐水(500mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:10)纯化得到4-(2,6-二氧哌啶-3-基)。Methyl 4-(4-cyano-1-methoxy-1-oxobutan-2-yl)benzoate (8.5 g, 32.56 mmol) was dissolved in acetic acid (30 mL), sulfuric acid (15 mL) was added, Stir at 110 °C for 12 h, extract with dichloromethane/methanol (10/1, 150 ml × 3), wash the organic phase with saturated brine (500 mL), dry over anhydrous sodium sulfate, filter, and concentrate under reduced pressure. The crude product was subjected to column chromatography ( MeOH:DCM=1:10) was purified to give 4-(2,6-dioxopiperidin-3-yl).
1H NMR(400MHz,DMSO-d 6)δ12.89(s,1H),10.89(s,1H),7.91(d,J＝4.0Hz,2H),7.36(d,J＝4.0Hz,2H),4.02-3.92(m,1H),2.72-2.63(m,1H),2.56-2.45(m,1H),2.30-2.20(m,1H),2.10-2.00(m,1H). 1 H NMR (400MHz, DMSO-d 6 ) δ 12.89(s, 1H), 10.89(s, 1H), 7.91(d, J=4.0Hz, 2H), 7.36(d, J=4.0Hz, 2H) ,4.02-3.92(m,1H),2.72-2.63(m,1H),2.56-2.45(m,1H),2.30-2.20(m,1H),2.10-2.00(m,1H).
步骤3：4-(2,6-二氧代基哌啶-3-基)苯甲酸五氟苯酯的制备Step 3: Preparation of Pentafluorophenyl 4-(2,6-dioxopiperidin-3-yl)benzoate
Figure PCTCN2022088560-appb-000612
Figure PCTCN2022088560-appb-000612
将4-(2,6-二氧哌啶-3-基)苯甲酸(1.3g,5.579mmol)用DMF(100mL)溶解，加入五氟苯酚(1.129g,6.14mmol)和DCC(1.265g，6.14mmol)，室温搅拌过夜，用乙酸乙酯(100mL×3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝3:7)纯化得到4-(2,6-二氧代基哌啶-3-基)苯甲酸五氟苯酯。4-(2,6-Dioxypiperidin-3-yl)benzoic acid (1.3 g, 5.579 mmol) was dissolved in DMF (100 mL), pentafluorophenol (1.129 g, 6.14 mmol) and DCC (1.265 g, 6.14 mmol), stirred at room temperature overnight, extracted with ethyl acetate (100 mL×3), washed the organic phase with saturated brine (150 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (EA: PE=3:7) was purified to give pentafluorophenyl 4-(2,6-dioxopiperidin-3-yl)benzoate.
1H NMR(400MHz,DMSO-d 6)δ10.95(s,1H),8.17(d,J＝4.0Hz,2H),7.56(d,J＝4.0Hz,2H),4.14-4.08(m,1H),2.79-2.69(m,1H),2.66-2.55(m,1H),2.30-2.23(m,1H),2.15-2.05(m,1H). 1 H NMR (400MHz, DMSO-d 6 )δ10.95(s, 1H), 8.17(d, J=4.0Hz, 2H), 7.56(d, J=4.0Hz, 2H), 4.14-4.08(m, 1H), 2.79-2.69(m, 1H), 2.66-2.55(m, 1H), 2.30-2.23(m, 1H), 2.15-2.05(m, 1H).
中间体18：3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯Intermediate 18: Pentafluorophenyl 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoate
步骤1：3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸的制备Step 1: Preparation of 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid
Figure PCTCN2022088560-appb-000613
Figure PCTCN2022088560-appb-000613
将3-氨基-4-甲氧基苯甲酸(5.0g,2.93mmol)悬浮于丙烯酸(8.05mL,117mmol)中，并在100℃下搅拌反应3h，然后将反应液搅拌冷却至室温。加入乙酸(33ml)，将搅拌的悬浮液在100℃加热10分钟，加入尿素(11.00g,183mmol)，反应液在120℃搅拌过夜。将反应液加入到冰水和浓盐酸(37％)的混合液中，搅拌，将得到的悬浮液在5℃的冰箱中保存过夜，然后过滤，固体用水洗涤并干燥，得到固体。将固体在盐酸溶液(0.05M)中研磨，过滤，甲基叔丁基醚洗涤，40℃下减压干燥，得到目标产物。3-Amino-4-methoxybenzoic acid (5.0 g, 2.93 mmol) was suspended in acrylic acid (8.05 mL, 117 mmol), and the reaction was stirred at 100° C. for 3 h, and then the reaction solution was stirred and cooled to room temperature. Acetic acid (33 ml) was added, the stirred suspension was heated at 100°C for 10 minutes, urea (11.00 g, 183 mmol) was added and the reaction was stirred at 120°C overnight. The reaction solution was added to a mixture of ice water and concentrated hydrochloric acid (37%), stirred, and the resulting suspension was stored in a refrigerator at 5°C overnight, then filtered, and the solid was washed with water and dried to obtain a solid. The solid was triturated in hydrochloric acid solution (0.05M), filtered, washed with methyl tert-butyl ether, and dried under reduced pressure at 40°C to give the desired product.
1H NMR(400MHz,DMSO-d 6)δ12.70(s,1H),10.34(s,1H),7.92(dd,J＝8.6,2.2Hz,1H),7.83(d,J＝2.2Hz,1H),7.21(d,J＝8.8Hz,1H),3.94-3.82(m,3H),3.60(t,J＝6.7Hz,2H),2.69(s,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 12.70 (s, 1H), 10.34 (s, 1H), 7.92 (dd, J=8.6, 2.2Hz, 1H), 7.83 (d, J=2.2Hz, 1H), 7.21(d, J=8.8Hz, 1H), 3.94-3.82(m, 3H), 3.60(t, J=6.7Hz, 2H), 2.69(s, 2H).
步骤2：3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯的制备Step 2: Preparation of 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester
Figure PCTCN2022088560-appb-000614
Figure PCTCN2022088560-appb-000614
3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸(2.0g,7.58mmol)，2,3,4,5,6-五氟苯酚(1.67g,9.09mmol)和N,N'-二环己基碳酰亚胺(1.87g,9.09mmol)在N,N-二甲基甲酰胺(20mL)溶液中的混合物在室温下搅拌反应3h。将反应液倒入水(200mL)中并搅拌0.5h，溶液用乙酸乙酯(200mL×3)萃取。收集有机相，并用水(500mL×2)和饱和食盐水(300mL)洗涤，用无水硫酸钠干燥，过滤并浓缩。浓缩物经柱层析纯化，得到目标产物3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯。3-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid (2.0 g, 7.58 mmol), 2,3,4,5,6-pentafluoro A mixture of phenol (1.67 g, 9.09 mmol) and N,N'-dicyclohexylcarbonimide (1.87 g, 9.09 mmol) in N,N-dimethylformamide (20 mL) was stirred at room temperature 3h. The reaction solution was poured into water (200 mL) and stirred for 0.5 h, and the solution was extracted with ethyl acetate (200 mL×3). The organic phase was collected, washed with water (500 mL×2) and saturated brine (300 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by column chromatography to obtain the target product, 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester.
LC-MS:(ESI,m/z):[M+H] +＝431.1. LC-MS: (ESI, m/z): [M+H] + = 431.1.
中间体19：3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-氟苯甲酸五氟苯酯Intermediate 19: Pentafluorophenyl 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoate
Figure PCTCN2022088560-appb-000615
Figure PCTCN2022088560-appb-000615
参照中间体18的方法制备。Prepared according to the method of Intermediate 18.
LC-MS:(ESI,m/z):[M+H] +＝419.0. LC-MS: (ESI, m/z): [M+H] + = 419.0.
中间体20：3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯Intermediate 20: Pentafluorophenyl 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate
Figure PCTCN2022088560-appb-000616
Figure PCTCN2022088560-appb-000616
参照中间体18的方法制备。Prepared according to the method of Intermediate 18.
LC-MS:(ESI,m/z):[M+H] +＝401.0. LC-MS: (ESI, m/z): [M+H] + = 401.0.
中间体21：(1R,4R)-4-(4-(((R)-1-(4-(2-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯Intermediate 21: (1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
步骤1：(1R,4R)-4-(4-(((R)-1-(4-(2-甲酰基苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 1: (1R,4R)-4-(4-(((R)-1-(4-(2-formylphenyl)thiophen-2-yl)ethyl)amino)-7-methoxy - Preparation of methyl 2-methylquinazolin-6-yl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000617
Figure PCTCN2022088560-appb-000617
向(1R,4R)-4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(250mg,0.48mmol)的1,4-二氧六环/H 2O(1.5mL/0.5mL)溶液中加K 3PO 4(255mg,1.2mmol),(PPh 3) 2PdCl 2(34mg,0.048mmol)和(2-甲酰基苯基)硼酸(87mg,0.58mmol)。反应液在100℃搅拌过夜。反应液浓缩，然后经层析柱(PE/EA＝2/1～1/2)纯化得到(1R,4R)-4-(4-(((R)-1-(4-(2-甲酰基苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 To (1R,4R)-4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- To a solution of methyl 6-yl)cyclohexane-1-carboxylate (250 mg, 0.48 mmol) in 1,4-dioxane/H 2 O (1.5 mL/0.5 mL) was added K 3 PO 4 (255 mg, 1.2 mmol), ( PPh3 ) 2PdCl2 (34 mg, 0.048 mmol) and ( 2 -formylphenyl)boronic acid (87 mg, 0.58 mmol). The reaction solution was stirred at 100°C overnight. The reaction solution was concentrated, and then purified by chromatography column (PE/EA=2/1～1/2) to obtain (1R,4R)-4-(4-(((R)-1-(4-(2-methyl) Acylphenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝544.1. LC-MS: (ESI, m/z): [M+H] + = 544.1.
步骤2：(1R,4R)-4-(4-(((R)-1-(4-(2-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 2: (1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl) preparation of cyclohexane-1-carboxylic acid methyl ester
Figure PCTCN2022088560-appb-000618
Figure PCTCN2022088560-appb-000618
向(1R,4R)-4-(4-(((R)-1-(4-(2-甲酰基苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(200mg,0.36mmol)和二甲基胺盐酸(60mg,0.74mmol)混合物中加MeOH(3mL)，DCE(3mL)和AcOH(5滴)。上述溶液在室温搅拌1h后，加入NaBH 3CN(46mg,0.74mmol)然后反应液在室温继续搅拌3h。反应液中加入DCM和水，分离有机相，经无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经Prep-HPLC纯化得到(1R,4R)-4-(4-(((R)-1-(4-(2-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 To (1R,4R)-4-(4-(((R)-1-(4-(2-formylphenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (200mg, 0.36mmol) and dimethylamine hydrochloric acid (60mg, 0.74mmol) To the mixture was added MeOH (3mL), DCE (3mL) ) and AcOH (5 drops). After the above solution was stirred at room temperature for 1 h, NaBH 3 CN (46 mg, 0.74 mmol) was added and the reaction solution was further stirred at room temperature for 3 h. DCM and water were added to the reaction solution, the organic phase was separated, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by Prep-HPLC to give (1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝573.3 LC-MS: (ESI, m/z): [M+H] + = 573.3
1H NMR(400MHz,CDCl 3)δ7.44-7.34(m,3H),7.33-7.28(m,4H),7.12(s,1H),6.11-6.02(m,1H),5.69-5.60(m,1H),3.92(s,3H),3.69(s,3H),3.38(s,2H),3.04-2.98(m,1H),2.63(s,3H),2.44-2.33(m,1H),2.24-2.18(m,6H),2.16-2.07(m,2H),2.05-1.95(m,2H),1.82-1.79(d,J＝6.8Hz,3H),1.67-1.60(m,4H). 1 H NMR (400MHz, CDCl 3 ) δ 7.44-7.34(m, 3H), 7.33-7.28(m, 4H), 7.12(s, 1H), 6.11-6.02(m, 1H), 5.69-5.60(m ,1H),3.92(s,3H),3.69(s,3H),3.38(s,2H),3.04-2.98(m,1H),2.63(s,3H),2.44-2.33(m,1H), 2.24-2.18(m, 6H), 2.16-2.07(m, 2H), 2.05-1.95(m, 2H), 1.82-1.79(d, J=6.8Hz, 3H), 1.67-1.60(m, 4H).
中间体22：4-(3-溴丙-1-炔-1-基)哌啶-1-羧酸叔丁酯Intermediate 22: tert-butyl 4-(3-bromoprop-1-yn-1-yl)piperidine-1-carboxylate
步骤1：4-(2,2-二溴乙烯基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000619
Figure PCTCN2022088560-appb-000619
0℃时搅拌下，向CBr 4(14.0g,42.24mmol)的DCM(200mL)溶液中加入PPh 3(22.13g,84.48mmol)，并在0℃时继续搅拌30min，然后加入4-醛基哌啶-1-羧酸叔丁酯(6.0g,28.16mmol)，反应液在室温搅拌过夜。反应液用EA(200mL)稀释，然后过滤。滤液减压浓缩。所得粗品经flash柱(EA:PE＝0～3:7)得到4-(2,2-二溴乙烯基)哌啶-1-羧酸叔丁酯。 To a solution of CBr 4 (14.0 g, 42.24 mmol) in DCM (200 mL) was added PPh 3 (22.13 g, 84.48 mmol) with stirring at 0 °C, and stirring was continued for 30 min at 0 ° C, followed by the addition of 4-aldopiperidine tert-butyl pyridine-1-carboxylate (6.0 g, 28.16 mmol), the reaction solution was stirred at room temperature overnight. The reaction solution was diluted with EA (200 mL), then filtered. The filtrate was concentrated under reduced pressure. The obtained crude product was passed through a flash column (EA:PE=0～3:7) to obtain tert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M-tBu] +＝313.9. LC-MS: (ESI, m/z): [M-tBu] + = 313.9.
步骤2：4-(3-羟基丙-1-炔-1-基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000620
Figure PCTCN2022088560-appb-000620
-78℃下，向4-(2,2-二溴乙烯基)哌啶-1-羧酸叔丁酯(4.0g,10.86mmol)的THF(60mL)溶液中加入n-BuLi(13.6mL,1.6M/正己烷)。混合液在-78℃搅拌1h后，加入多聚甲醛(977mg,32.60mmol)。反应液 在室温搅拌过夜。反应液中加入NH 4Cl(100mL)淬灭反应，并用EA(100mL×3)萃取，合并有机相并用饱和食盐水(300mL)洗涤，无水Na 2SO 4干燥，过滤并浓缩。所得粗品经flash柱(EA:PE＝0～4:1)纯化得到4-(3-羟基丙-1-炔-1-基)哌啶-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylate (4.0 g, 10.86 mmol) in THF (60 mL) at -78°C was added n-BuLi (13.6 mL, 1.6M/n-hexane). After the mixture was stirred at -78°C for 1 h, paraformaldehyde (977 mg, 32.60 mmol) was added. The reaction solution was stirred at room temperature overnight. NH 4 Cl (100 mL) was added to the reaction solution to quench the reaction, and extracted with EA (100 mL×3). The organic phases were combined and washed with saturated brine (300 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The obtained crude product was purified by flash column (EA:PE=0～4:1) to obtain tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M-Boc] +＝140.2. LC-MS: (ESI, m/z): [M-Boc] + = 140.2.
1H NMR(400MHz,DMSO-d 6)δ5.04(t,J＝5.9Hz,1H),4.04(dd,J＝5.8,2.0Hz,2H),3.65–3.55(m,2H),3.04(t,J＝10.1Hz,2H),2.60(ddd,J＝8.8,7.0,3.5Hz,1H),1.77–1.64(m,2H),1.43–1.31(m,11H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 5.04 (t, J=5.9 Hz, 1H), 4.04 (dd, J=5.8, 2.0 Hz, 2H), 3.65-3.55 (m, 2H), 3.04 ( t, J=10.1Hz, 2H), 2.60 (ddd, J=8.8, 7.0, 3.5Hz, 1H), 1.77–1.64 (m, 2H), 1.43–1.31 (m, 11H).
步骤3：4-(3-溴丙-1-炔-1-基)哌啶-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(3-bromoprop-1-yn-1-yl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000621
Figure PCTCN2022088560-appb-000621
0℃时，边搅拌边向4-(3-羟基丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(700mg,2.92mmol)和PPh 3(1.94g,5.83mmol)的DCM(10mL)溶液中加入CBr 4(1.94g,5.83mmol)。反应液在室温搅拌过夜。反应液中加入EA(10mL)稀释，然后过滤。滤液减压浓缩。所得粗品经flash柱(EA:PE＝0～3:7)纯化得到4-(3-溴丙-1-炔-1-基)哌啶-1-羧酸叔丁酯。 At 0 °C, tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate (700 mg, 2.92 mmol) and PPh 3 (1.94 g, 5.83 mmol) were added with stirring. To a solution of DCM (10 mL) was added CBr4 (1.94 g, 5.83 mmol). The reaction solution was stirred at room temperature overnight. EA (10 mL) was added to the reaction solution to dilute, and then filtered. The filtrate was concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～3:7) to obtain tert-butyl 4-(3-bromoprop-1-yn-1-yl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M-tBu] +＝246.0. LC-MS: (ESI, m/z): [M-tBu] + = 246.0.
1H NMR(400MHz,DMSO-d 6)δ4.24(d,J＝2.0Hz,2H),3.64–3.54(m,2H),3.13–3.00(m,2H),2.75–2.65(m,1H),1.78–1.68(m,2H),1.44–1.33(m,11H). 1 H NMR (400MHz, DMSO-d 6 )δ4.24(d, J=2.0Hz, 2H), 3.64-3.54(m, 2H), 3.13-3.00(m, 2H), 2.75-2.65(m, 1H) ), 1.78–1.68 (m, 2H), 1.44–1.33 (m, 11H).
中间体23：4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯Intermediate 23: tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate
步骤1：4-(2-(吡啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(2-(pyridin-4-ylmethoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000622
Figure PCTCN2022088560-appb-000622
0℃时，向4-(2-羟基乙基)哌啶-1-羧酸叔丁酯(1.0g,4.36mmol)的THF(20mL)溶液中加入NaH(60％,1.2g,30.58mmol)，并在0℃搅拌20分钟，升至室温后，加入4-(溴甲基)吡啶溴化氢(1.3g,5.13mmol)，然后反应混合物于室温下搅拌反应过夜。反应液中加入水(30mL)，EA(30mL×3)萃取，合并有机相并用食盐水洗(30mL)，Na 2SO 4干燥，减压浓缩。浓缩物经flash柱纯化(EA:PE＝0～4:1)得到目标产物4-(2-(吡啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate (1.0 g, 4.36 mmol) in THF (20 mL) at 0 °C was added NaH (60%, 1.2 g, 30.58 mmol) , and stirred at 0° C. for 20 minutes. After warming to room temperature, 4-(bromomethyl)pyridine hydrogen bromide (1.3 g, 5.13 mmol) was added, and then the reaction mixture was stirred at room temperature overnight. Water (30 mL) was added to the reaction solution, extracted with EA (30 mL×3), the organic phases were combined and washed with brine (30 mL), dried over Na 2 SO 4 , and concentrated under reduced pressure. The concentrate was purified by flash column (EA:PE=0～4:1) to obtain the target product tert-butyl 4-(2-(pyridin-4-ylmethoxy)ethyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝321.1. LC-MS: (ESI, m/z): [M+H] + = 321.1.
1H NMR(400MHz,CDCl 3)δ8.57(d,J＝5.9Hz,2H),7.24(d,J＝5.7Hz,2H),4.51(s,2H),4.09(d,J＝15.9Hz,2H),3.55(t,J＝6.1Hz,2H),2.70(t,J＝12.2Hz,2H),1.66(d,J＝13.9Hz,2H),1.58(m,2H),1.45(s,9H),1.26(m,1H),1.13(d,J＝8.4Hz,2H). 1 H NMR (400 MHz, CDCl 3 ) δ 8.57 (d, J=5.9 Hz, 2H), 7.24 (d, J=5.7 Hz, 2H), 4.51 (s, 2H), 4.09 (d, J=15.9 Hz ,2H),3.55(t,J＝6.1Hz,2H),2.70(t,J＝12.2Hz,2H),1.66(d,J＝13.9Hz,2H),1.58(m,2H),1.45(s ,9H),1.26(m,1H),1.13(d,J=8.4Hz,2H).
步骤2：4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000623
Figure PCTCN2022088560-appb-000623
将4-(2-(吡啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(1.9g,5.9mmol)和Pd/C(570mg)在i-PrOH/H 2O(30mL/35mL)中的混合液在75℃下搅拌过夜。反应液经硅藻土过滤，滤液浓缩得到目标产物4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯。所得产物无需纯化，直接用于下一步反应。 4-(2-(Pyridin-4-ylmethoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (1.9 g, 5.9 mmol) and Pd/C (570 mg) in i - PrOH/H The mixture in O (30 mL/35 mL) was stirred at 75°C overnight. The reaction solution was filtered through celite, and the filtrate was concentrated to obtain the target product, tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate. The obtained product was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝327.2. LC-MS: (ESI, m/z): [M+H] + = 327.2.
中间体24：2-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)乙醛Intermediate 24: 2-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)piperidin-4 - base) acetaldehyde
步骤1：2-(2,6-二氧代基哌啶-3-基)-4-(4-(2-羟基乙基)哌啶-1-基)异吲哚啉-1,3-二酮的制备Step 1: 2-(2,6-Dioxopiperidin-3-yl)-4-(4-(2-hydroxyethyl)piperidin-1-yl)isoindoline-1,3- Preparation of diketones
Figure PCTCN2022088560-appb-000624
Figure PCTCN2022088560-appb-000624
向2-(2,6-二氧代基哌啶-3-基)-4-氟异吲哚啉-1,3-二酮(1.0g,3.6mmol)的DMF(10mL)溶液中加2-(哌啶-4-基)乙烷-1-醇(467mg,3.6mmol)和DIEA(1.4g,10.8mmol)。反应液在100℃搅拌过夜。反应液中加水(100mL)淬灭反应。然后用EA(20mL×3)萃取。合并有机相用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(EA:PE＝0～1:1)纯化得到2-(2,6-二氧代基哌啶-3-基)-4-(4-(2-羟基乙基)哌啶-1-基)异吲哚啉-1,3-二酮。 To a solution of 2-(2,6-dioxopiperidin-3-yl)-4-fluoroisoindoline-1,3-dione (1.0 g, 3.6 mmol) in DMF (10 mL) was added 2 -(piperidin-4-yl)ethan-1-ol (467 mg, 3.6 mmol) and DIEA (1.4 g, 10.8 mmol). The reaction solution was stirred at 100°C overnight. Water (100 mL) was added to the reaction solution to quench the reaction. It was then extracted with EA (20 mL x 3). The combined organic phases were washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～1:1) to obtain 2-(2,6-dioxopiperidin-3-yl)-4-(4-(2-hydroxyethyl)piperidine pyridin-1-yl)isoindoline-1,3-dione.
LC-MS:(ESI,m/z):[M+H] +＝386.1. LC-MS: (ESI, m/z): [M+H] + = 386.1.
步骤2：2-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)乙醛的制备Step 2: 2-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)piperidin-4- Preparation of acetaldehyde
Figure PCTCN2022088560-appb-000625
Figure PCTCN2022088560-appb-000625
边搅拌边向2-(2,6-二氧代基哌啶-3-基)-4-(4-(2-羟基乙基)哌啶-1-基)异吲哚啉-1,3-二酮(1.1g,3.0mmol)的ACN(20mL)溶液中加IBX(1.7g,6.0mmol)。反应液在80℃搅拌2h。反应液过滤，滤液浓缩。所得粗品经flash柱(EA:PE＝0～1:1)纯化得到2-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)乙醛。To 2-(2,6-dioxopiperidin-3-yl)-4-(4-(2-hydroxyethyl)piperidin-1-yl)isoindoline-1,3 with stirring - To a solution of the diketone (1.1 g, 3.0 mmol) in ACN (20 mL) was added IBX (1.7 g, 6.0 mmol). The reaction solution was stirred at 80°C for 2h. The reaction solution was filtered, and the filtrate was concentrated. The obtained crude product was purified by flash column (EA:PE=0～1:1) to obtain 2-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxo) ylisoindolin-4-yl)piperidin-4-yl)acetaldehyde.
LC-MS:(ESI,m/z):[M+H] +＝384.0. LC-MS: (ESI, m/z): [M+H] + = 384.0.
1H NMR(400MHz,DMSO-d 6)δ11.08(s,1H),9.72(s,1H),7.77–7.58(m,1H),7.34(dd,J＝7.7,4.9Hz,2H),5.09(dd,J＝12.9,5.4Hz,1H),3.68(d,J＝11.8Hz,2H),2.97-2.82(m,3H),2.64–2.53(m,2H),2.45(d,J＝6.6Hz,2H),2.13–1.99(m,3H),1.82-1.72(m,2H),1.50-1.30(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 11.08 (s, 1H), 9.72 (s, 1H), 7.77-7.58 (m, 1H), 7.34 (dd, J=7.7, 4.9Hz, 2H), 5.09(dd,J＝12.9,5.4Hz,1H),3.68(d,J＝11.8Hz,2H),2.97-2.82(m,3H),2.64-2.53(m,2H),2.45(d,J＝ 6.6Hz, 2H), 2.13-1.99(m, 3H), 1.82-1.72(m, 2H), 1.50-1.30(m, 2H).
中间体25：3-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)丙醛Intermediate 25: 3-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)piperidin-4 -yl) propionaldehyde
步骤1：3-(哌啶-4-基)丙烷-1-醇的制备Step 1: Preparation of 3-(piperidin-4-yl)propan-1-ol
Figure PCTCN2022088560-appb-000626
Figure PCTCN2022088560-appb-000626
向4-(3-羟基丙基)哌啶-1-羧酸叔丁酯(930.0mg,3,8mmol)的DCM(8.00mL)中加TFA(4.0mL)。反应液室温搅拌过夜。反应液直接浓缩得到3-(哌啶-4-基)丙烷-1-醇。所得粗品直接用于下一步反应。To tert-butyl 4-(3-hydroxypropyl)piperidine-1-carboxylate (930.0 mg, 3,8 mmol) in DCM (8.00 mL) was added TFA (4.0 mL). The reaction solution was stirred at room temperature overnight. The reaction solution was directly concentrated to obtain 3-(piperidin-4-yl)propan-1-ol. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝144.2. LC-MS: (ESI, m/z): [M+H] + = 144.2.
步骤2：2-(2,6-二氧代基哌啶-3-基)-4-(4-(3-羟基丙基)哌啶-1-基)异吲哚啉-1,3-二酮的制备Step 2: 2-(2,6-Dioxopiperidin-3-yl)-4-(4-(3-hydroxypropyl)piperidin-1-yl)isoindoline-1,3- Preparation of diketones
Figure PCTCN2022088560-appb-000627
Figure PCTCN2022088560-appb-000627
边搅拌边向3-(哌啶-4-基)丙烷-1-醇(730mg,TFAsalt,3.8mmol)的DMF(10mL)溶液中加2-(2,6-二氧代基哌啶-3-基)-4-氟异吲哚啉-1,3-二酮(1.0g,3.8mmol)和DIEA(1.5g,11.4mmol)。反应液在100℃搅拌过夜。反应液中加水(100mL)淬灭反应。然后用EA(20mL×3)萃取。有机相用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，浓缩。所得粗品经flash柱(EA:PE＝0～1:1)纯化得到2-(2,6-二氧代基哌啶-3-基)-4-(4-(3-羟基丙基)哌啶-1-基)异吲哚啉-1,3-二酮。 To a solution of 3-(piperidin-4-yl)propan-1-ol (730 mg, TFAsalt, 3.8 mmol) in DMF (10 mL) was added 2-(2,6-dioxopiperidine-3 with stirring) -yl)-4-fluoroisoindoline-1,3-dione (1.0 g, 3.8 mmol) and DIEA (1.5 g, 11.4 mmol). The reaction solution was stirred at 100°C overnight. Water (100 mL) was added to the reaction solution to quench the reaction. It was then extracted with EA (20 mL x 3). The organic phase was washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The obtained crude product was purified by flash column (EA:PE=0～1:1) to obtain 2-(2,6-dioxopiperidin-3-yl)-4-(4-(3-hydroxypropyl)piperidine pyridin-1-yl)isoindoline-1,3-dione.
LC-MS:(ESI,m/z):[M+H] +＝400.0. LC-MS: (ESI, m/z): [M+H] + =400.0.
步骤3：3-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)丙醛的制备Step 3: 3-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)piperidin-4- Preparation of yl) propionaldehyde
Figure PCTCN2022088560-appb-000628
Figure PCTCN2022088560-appb-000628
边搅拌边向2-(2,6-二氧代基哌啶-3-基)-4-(4-(3-羟基丙基)哌啶-1-基)异吲哚啉-1,3-二酮(700mg,1.7mmol)的ACN(20mL)溶液中加IBX(982mg,3.5mmol)。反应液在80℃搅拌2h。反应液过滤，滤液浓缩。所得粗品经flash柱(EA:PE＝0～1:1)纯化得到3-(1-(2-(2,6-二氧代基哌啶-3-基)-1,3-二氧代基异吲哚啉-4-基)哌啶-4-基)丙醛。To 2-(2,6-dioxopiperidin-3-yl)-4-(4-(3-hydroxypropyl)piperidin-1-yl)isoindoline-1,3 with stirring - To a solution of the diketone (700 mg, 1.7 mmol) in ACN (20 mL) was added IBX (982 mg, 3.5 mmol). The reaction solution was stirred at 80°C for 2h. The reaction solution was filtered, and the filtrate was concentrated. The obtained crude product was purified by flash column (EA:PE=0～1:1) to obtain 3-(1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxo) ylisoindolin-4-yl)piperidin-4-yl)propanal.
LC-MS:(ESI,m/z):[M+H] +＝398.0. LC-MS: (ESI, m/z): [M+H] + = 398.0.
1H NMR(400MHz,DMSO-d 6)δ11.08(s,1H),9.71(t,J＝1.4Hz,1H),7.74–7.60(m,1H),7.33(dd,J＝7.7,3.4Hz,2H),5.09(dd,J＝12.9,5.4Hz,1H),3.69(d,J＝11.9Hz,2H),2.93-2.79(m,3H),2.64–2.46(m,4H),2.07–2.00(m,1H),1.80-1.72(m,2H),1.54(dd,J＝14.0,7.1Hz,2H),1.40-1.27(m,3H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 11.08 (s, 1H), 9.71 (t, J=1.4 Hz, 1H), 7.74-7.60 (m, 1H), 7.33 (dd, J=7.7, 3.4 Hz, 2H), 5.09(dd, J＝12.9, 5.4Hz, 1H), 3.69(d, J＝11.9Hz, 2H), 2.93-2.79(m, 3H), 2.64-2.46(m, 4H), 2.07 –2.00(m,1H),1.80-1.72(m,2H),1.54(dd,J=14.0,7.1Hz,2H),1.40-1.27(m,3H).
中间体26：9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯Intermediate 26: Benzyl 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate
步骤1：9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: 9-((4-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 - Preparation of tert-butyl carboxylate
Figure PCTCN2022088560-appb-000629
Figure PCTCN2022088560-appb-000629
将9-醛基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.0g,3.56mmol)和(9H-芴-9-基)甲基哌嗪-1-羧酸酯(1.35g,3.91mmol)溶于THF(20mL)中，加入STAB(2.26g,10.68mmol)，室温搅拌过夜，加水(100mL)，用乙酸乙酯(100mLx3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA/PE＝3:2)纯化得到9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。9-Aldol-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (1.0 g, 3.56 mmol) and (9H-fluoren-9-yl)methylpiperazine-1-carboxylate The acid ester (1.35g, 3.91mmol) was dissolved in THF (20mL), STAB (2.26g, 10.68mmol) was added, stirred at room temperature overnight, added water (100mL), extracted with ethyl acetate (100mL×3), saturated brine (150mL) ) washed the organic phase, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (EA/PE=3:2) to obtain 9-((4-(((9H-fluoren-9-yl )methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝574.2. LC-MS: (ESI, m/z): [M+H] + = 574.2.
步骤2：(9H-芴-9-基)甲基4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸酯的制备Step 2: Preparation of (9H-fluoren-9-yl)methyl 4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000630
Figure PCTCN2022088560-appb-000630
将9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.1g,1.92mmol)溶解在DCM(10mL)中，加入TFA(2mL)，室温搅拌1h，减压浓缩，得到(9H-芴-9-基)甲基4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸酯，直接用于下一步。9-((4-(((9H-fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxy tert-Butyl acid (1.1 g, 1.92 mmol) was dissolved in DCM (10 mL), TFA (2 mL) was added, stirred at room temperature for 1 h, and concentrated under reduced pressure to give (9H-fluoren-9-yl)methyl 4-((3 - Azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate, used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝474.1. LC-MS: (ESI, m/z): [M+H] + = 474.1.
步骤3：9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的制备Step 3: 9-((4-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 - Preparation of benzyl carboxylate
Figure PCTCN2022088560-appb-000631
Figure PCTCN2022088560-appb-000631
将(9H-芴-9-基)甲基4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸酯(1.1g,2.33mmol)溶于ACN(20mL)中，加入NaHCO 3饱和溶液(20mL)，搅拌下加入CbzCl(0.60g,3.50mmol)，室温下反应过夜。减压浓缩除去乙腈，加水(50mL)，用乙酸乙酯(100mLx3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA/PE＝11:9)纯化得到9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯。 (9H-Fluoren-9-yl)methyl 4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate (1.1 g, 2.33 mmol) It was dissolved in ACN (20 mL), a saturated solution of NaHCO 3 (20 mL) was added, CbzCl (0.60 g, 3.50 mmol) was added under stirring, and the reaction was carried out overnight at room temperature. Concentrated under reduced pressure to remove acetonitrile, added water (50 mL), extracted with ethyl acetate (100 mL×3), washed the organic phase with saturated brine (150 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (EA /PE=11:9) purification to obtain 9-((4-(((9H-fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5 ] Benzyl undecane-3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝608.1. LC-MS: (ESI, m/z): [M+H] + = 608.1.
步骤4：9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的制备Step 4: Preparation of benzyl 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000632
Figure PCTCN2022088560-appb-000632
将9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(0.97g,1.60mmol)溶于CAN(10Ml)中，加入哌啶(2mL)，室温搅拌3h。减压浓缩除去溶剂，加水(50mL)，用乙酸乙酯(100mLx3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层柱(MeOH/DCM＝3:17)纯化得到9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯。9-((4-(((9H-fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxy Benzyl acid (0.97 g, 1.60 mmol) was dissolved in CAN (10 Ml), piperidine (2 mL) was added, and the mixture was stirred at room temperature for 3 h. Concentrate under reduced pressure to remove the solvent, add water (50 mL), extract with ethyl acetate (100 mL×3), wash the organic phase with saturated brine (150 mL), dry over anhydrous sodium sulfate, filter, and concentrate under reduced pressure. /DCM=3:17) was purified to give benzyl 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝386.1. LC-MS: (ESI, m/z): [M+H] + = 386.1.
中间体27：4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯Intermediate 27: Methyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
步骤1：4-(((三氟甲氧基)磺酰基)氧)环己-3-烯-1-羧酸甲酯的制备Step 1: Preparation of methyl 4-(((trifluoromethoxy)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000633
Figure PCTCN2022088560-appb-000633
将2,6-二甲基-1λ 2-哌嗪(51.4g,480.37mmol)和Tf 2O(90.38g,320.50mmol)加入到4-氧代环己烷-1-羧酸甲酯(50.0g,320.51mmol)的二氯甲烷(500ml)中，0℃搅拌1h，再补加Tf 2O(72.3g,256.38mmol)，常 温下搅拌过夜，用水洗，无水硫酸钠干燥，减压浓缩，粗品用柱层析(PE:EA＝5:1)得到4-(((三氟甲氧基)磺酰基)氧)环己-3-烯-1-羧酸甲酯。 2,6-Dimethyl-1λ 2 -piperazine (51.4 g, 480.37 mmol) and Tf 2 O (90.38 g, 320.50 mmol) were added to methyl 4-oxocyclohexane-1-carboxylate (50.0 g, 320.51 mmol) in dichloromethane (500 ml), stirred at 0 °C for 1 h, then added Tf 2 O (72.3 g, 256.38 mmol), stirred at room temperature overnight, washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure , the crude product was subjected to column chromatography (PE:EA=5:1) to obtain methyl 4-(((trifluoromethoxy)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate.
1H NMR(400MHz,DMSO-d 6)δ5.90(s,1H),3.63(s,3H),2.70–2.60(m,1H),2.47–2.28(m,4H),2.11–1.98(m,1H),1.81(tt,J＝8.9,6.0Hz,1H). 1 H NMR (400MHz, DMSO-d 6 )δ5.90(s,1H), 3.63(s,3H), 2.70-2.60(m,1H), 2.47-2.28(m,4H), 2.11-1.98(m ,1H),1.81(tt,J=8.9,6.0Hz,1H).
步骤2：4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯的制备Step 2: Preparation of methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000634
Figure PCTCN2022088560-appb-000634
将(Bpin) 2(39.1g,153.94mmol),Pd(dppf) 2Cl 2(7.5g,10.24mmol)和醋酸钾(30.4g,310.2mmol)加入到4-(((三氟甲氧基)磺酰基)氧)环己-3-烯-1-羧酸甲酯(30.0g,104.17mmol)的二氧六环(500ml)中，90℃搅拌过夜，反应液用水(2L)稀释，乙酸乙酯(500mL×3)萃取，饱和食盐水洗(500mL)，无水硫酸钠干燥，减压浓缩，粗品使用柱层析纯化(PE:EA＝0:100)得到4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯。 (Bpin) 2 (39.1 g, 153.94 mmol), Pd(dppf) 2 Cl 2 (7.5 g, 10.24 mmol) and potassium acetate (30.4 g, 310.2 mmol) were added to 4-(((trifluoromethoxy) Sulfonyl)oxy)cyclohex-3-ene-1-carboxylic acid methyl ester (30.0g, 104.17mmol) in dioxane (500ml), stirred at 90°C overnight, the reaction solution was diluted with water (2L), ethyl acetate Ester (500mL×3) was extracted, washed with saturated brine (500mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=0:100) to obtain 4-(4,4,5, Methyl 5-tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-ene-1-carboxylate.
1H NMR(400MHz,CDCl 3)δ6.53(s,1H),3.71–3.64(m,3H),2.61–2.46(m,1H),2.42–1.95(m,6H),1.28–1.19(m,12H). 1 H NMR (400MHz, CDCl 3 )δ6.53(s,1H), 3.71-3.64(m,3H), 2.61-2.46(m,1H), 2.42-1.95(m,6H), 1.28-1.19(m ,12H).
步骤3：4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 3: Preparation of methyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000635
Figure PCTCN2022088560-appb-000635
将4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯(25.0g,93.98mmol)，Pd(dppf) 2Cl 2(5.3g,7.24mmol)和Na 2CO 3(15.3g,144.34mmol)加入到6-溴-7-甲氧基-2-甲基喹唑啉-4-醇(19.4g,72.12mmol)的DMF/H 2O(300ml/30ml)中，110℃搅拌过夜，反应液用水(1L)稀释，乙酸乙酯(500mL×3)萃取，饱和食盐水(500mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(PE:EA＝0:100)纯化得到粗产品4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-ene-1-carboxylate (25.0 g, 93.98 g mmol), Pd(dppf)2Cl2 ( 5.3 g , 7.24 mmol) and Na2CO3 (15.3 g , 144.34 mmol) were added to 6-bromo-7-methoxy-2-methylquinazoline-4 -Alcohol (19.4g, 72.12mmol) in DMF/H 2 O (300ml/30ml), stirred at 110°C overnight, the reaction solution was diluted with water (1L), extracted with ethyl acetate (500mL×3), saturated brine (500mL) ) washed the organic phase, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=0:100) to obtain the crude product 4-(4-hydroxy-7-methoxy-2 -Methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝329.0. LC-MS: (ESI, m/z): [M+H] + = 329.0.
中间体28：(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯Intermediate 28: (1R,4R)-4-(7-Methoxy-2-methyl-4-(((R)-1-(4-(2-((methylamino)methyl)benzene yl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000636
Figure PCTCN2022088560-appb-000636
将(1R,4R)-4-(4-(((R)-1-(4-(2-醛基苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(180mg,0.33mmol)和甲胺溶液(0.33ml,0.66mmol,2M in THF)加到MeOH/DCE(2mL/2mL)中，再滴加几滴AcOH(4drops)。混合溶液在室温搅拌1h后，加入NaBH 3CN(42mg,0.66mmol)并继续搅拌反应3h。反应液中加入DCM和水，分离有机相，用无水Na 2SO 4干燥，过滤，减压浓缩。粗品经Prep-HPLC纯化得到(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯。 (1R,4R)-4-(4-(((R)-1-(4-(2-Aldolphenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (180mg, 0.33mmol) and methylamine solution (0.33ml, 0.66mmol, 2M in THF) were added to MeOH/DCE (2mL/ 2 mL), a few more drops of AcOH (4 drops) were added dropwise. After the mixed solution was stirred at room temperature for 1 h, NaBH 3 CN (42 mg, 0.66 mmol) was added and the reaction was continued to stir for 3 h. DCM and water were added to the reaction solution, the organic phase was separated, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The crude product was purified by Prep-HPLC to give (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(4-(2-((methylamino)methane) yl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝559.4. LC-MS: (ESI, m/z): [M+H] + = 559.4.
1H NMR(400MHz,CDCl 3)δ7.42-7.39(m,1H),7.35-7.26(m,5H),7.24-7.20(m,1H),7.10(s,1H),6.08-6.01(m,1H),5.65-5.60(m,1H),3.92(s,3H),3.73-3.69(m,5H),3.04-2.98(m,1H),2.63(s,3H),2.44-2.36(m,4H),2.14-1.99(m,4H),1.80(d,J＝6.8Hz,3H),1.70-1.53(m,4H). 1 H NMR (400MHz, CDCl 3 ) δ 7.42-7.39(m, 1H), 7.35-7.26(m, 5H), 7.24-7.20(m, 1H), 7.10(s, 1H), 6.08-6.01(m ,1H),5.65-5.60(m,1H),3.92(s,3H),3.73-3.69(m,5H),3.04-2.98(m,1H),2.63(s,3H),2.44-2.36(m ,4H),2.14-1.99(m,4H),1.80(d,J=6.8Hz,3H),1.70-1.53(m,4H).
实施例1：1-(5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 1: 1-(5-(9-(2-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-nitrogen Heterospiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000637
Figure PCTCN2022088560-appb-000637
((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(50mg,0.09mmol)，2-(3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)-3-氮杂螺[5.5]十一烷-9-基)乙醛(39mg,0.09mmol)和STAB(55mg,0.27mmol)在THF(2mL)溶液溶液中的混合物于25℃搅拌反应1小时。用水(50mL)淬灭反应，并用EA(50mL×3)萃取。收集有机层并用无水硫酸钠干燥，过滤并减压浓缩。浓缩物通过制备型HPLC(乙腈/0.08％碳酸氢铵水溶液中，5％至95％)纯化，得到1-(5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone (50 mg, 0.09 mmol), 2-(3-(4-chloro-3-(2,4-dioxo) yltetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)acetaldehyde (39 mg, 0.09 mmol) and STAB (55 mg, 0.27 mmol) in The mixture in solution in THF (2 mL) was stirred at 25°C for 1 hour. The reaction was quenched with water (50 mL) and extracted with EA (50 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by preparative HPLC (acetonitrile/0.08% aqueous ammonium bicarbonate, 5% to 95%) to give 1-(5-(9-(2-(4-((1R,4R)-4-( 4-(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl) Cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4( 1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1000.1. LC-MS: (ESI, m/z): [M+H] + = 1000.1.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.14–8.03(m,2H),7.64(d,J＝8.2Hz,1H),7.55(d,J＝1.6Hz,1H),7.39(d,J＝8.2Hz,1H),7.00(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.62–5.49(m,3H),3.89(s,3H),3.80–3.70(m,1H),3.67–3.42(m,7H),3.31–3.23(m,2H),2.99–2.88(m,1H),2.78–2.59(m,3H),2.40–2.25(m,9H),1.94–1.76(m,4H),1.74–1.20(m,18H),1.16–0.98(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.14-8.03 (m, 2H), 7.64 (d, J=8.2Hz, 1H), 7.55 (d, J=1.6Hz, 1H), 7.39(d, J=8.2Hz, 1H), 7.00(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.62–5.49(m, 3H) ),3.89(s,3H),3.80–3.70(m,1H),3.67–3.42(m,7H),3.31–3.23(m,2H),2.99–2.88(m,1H),2.78–2.59(m ,3H),2.40–2.25(m,9H),1.94–1.76(m,4H),1.74–1.20(m,18H),1.16–0.98(m,4H).
实施例2：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 2: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: 9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan- Preparation of tert-butyl 3-carboxylate
Figure PCTCN2022088560-appb-000638
Figure PCTCN2022088560-appb-000638
((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(140.0mg,0.2mmol)和9-甲酰基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(100.0mg,0.36mmol)在THF(6.0mL)溶液中的混合物中缓慢加入STAB(107mg,0.5mmol)。反应混合物在室温下搅拌反应过夜。用水(20.0mL)淬灭反应，并用EA(20.0mL×2)萃取。收集有机相并用无水硫酸钠干燥，减压浓缩，得到目标产物。粗产物可直接用于下一步。((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone (140.0 mg, 0.2 mmol) and 9-formyl-3-azaspiro[5.5]undecan-3- To a mixture of tert-butyl carboxylate (100.0 mg, 0.36 mmol) in THF (6.0 mL) was slowly added STAB (107 mg, 0.5 mmol). The reaction mixture was stirred at room temperature overnight. The reaction was quenched with water (20.0 mL) and extracted with EA (20.0 mL x 2). The organic phase was collected, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the desired product. The crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝836.2. LC-MS: (ESI, m/z): [M+H] + = 836.2.
步骤2：(4-(((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮Step 2: (4-(((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-(((( R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone
Figure PCTCN2022088560-appb-000639
Figure PCTCN2022088560-appb-000639
将9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(140mg,0.2mmol)在TFA/DCM(3.0mL,1:5)溶液中的混合物于室温下搅拌2小时。减压浓缩反应物，得到目标产物。粗产物直接用于下一步。9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- A mixture of tert-butyl carboxylate (140 mg, 0.2 mmol) in TFA/DCM (3.0 mL, 1:5) was stirred at room temperature for 2 hours. The reaction was concentrated under reduced pressure to obtain the target product. The crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝736.2. LC-MS: (ESI, m/z): [M+H] + = 736.2.
步骤3：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[ 5.5] Preparation of Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000640
Figure PCTCN2022088560-appb-000640
往(4-(((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(100mg,0.14mmol)在DMSO(5.0mL)溶液中的混合物中加入DIEA(54.2mg,0.42mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(73.0mg,0.17mmol)，反应混合物于室温下搅拌反应5.0小时。加入水(15.0mL)淬灭反应，并用EA(20mL×3)萃取，收集有机层，用饱和食盐水(20.0mL)洗涤，并经无水硫酸钠干燥。减压浓缩，浓缩物经制备型HPLC纯化，得到目标产物。To (4-(((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R) -1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone (100 mg , 0.14 mmol) in DMSO (5.0 mL) was added DIEA (54.2 mg, 0.42 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl ) pentafluorophenyl benzoate (73.0 mg, 0.17 mmol), the reaction mixture was stirred at room temperature for 5.0 hours. Water (15.0 mL) was added to quench the reaction, and extracted with EA (20 mL×3), the organic layer was collected and saturated with Washed with brine (20.0 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and purified by preparative HPLC to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝986.4. LC-MS: (ESI, m/z): [M+H] + = 986.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.16–8.02(m,2H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.38(d,J＝8.2Hz,1H),6.99(s,1H),6.87(s,1H),6.85(s,1H),6.70(s,1H),5.65-5.47(m,3H),3.88(s,3H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.51-3.42(m,4H),2.97-2.90(m,1H),2.78-2.72(m,2H),2.67-2.61(m,1H),2.39-2.23(m,7H),2.15-2.05(m,2H),1.87-1.78(m,4H),1.73–1.21(m,17H),1.17-0.98(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.16-8.02(m, 2H), 7.63(d, J=8.2Hz, 1H), 7.54(s, 1H), 7.38( d, J＝8.2Hz, 1H), 6.99(s, 1H), 6.87(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65-5.47(m, 3H), 3.88(s ,3H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.51-3.42(m,4H),2.97-2.90(m,1H),2.78-2.72(m,2H),2.67 -2.61(m, 1H), 2.39-2.23(m, 7H), 2.15-2.05(m, 2H), 1.87-1.78(m, 4H), 1.73-1.21(m, 17H), 1.17-0.98(m, 4H).
实施例3：1-(5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 3: 1-(5-(9-(2-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3,9 - Diazaspiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000641
Figure PCTCN2022088560-appb-000641
参照实施例2的方法制备。Prepare according to the method of Example 2.
LC-MS:(ESI,m/z):[M+H] +＝1001.3. LC-MS: (ESI, m/z): [M+H] + = 1001.3.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.09-8.06(m,2H),7.64(d,J＝8.1Hz,1H),7.55(s,1H),7.39(d,J＝7.6Hz,1H),7.00(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.65–5.47(m,3H),3.89(s,3H),3.82–3.40(m,9H),3.02–2.90(m,1H),2.82–2.71(m,2H),2.70–2.60(m,1H),2.46–2.24(m,15H),1.94–1.75(m,4H),1.73–1.26(m,16H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s,1H),8.09-8.06(m,2H),7.64(d,J=8.1Hz,1H),7.55(s,1H),7.39( d, J＝7.6Hz, 1H), 7.00(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.65–5.47(m, 3H), 3.89(s ,3H),3.82–3.40(m,9H),3.02–2.90(m,1H),2.82–2.71(m,2H),2.70–2.60(m,1H),2.46–2.24(m,15H),1.94 –1.75(m,4H),1.73–1.26(m,16H).
实施例4：(R)-1-(5-(9-((4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 4: (R)-1-(5-(9-((4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino )amino)-7-methoxy-2-methylquinazolin-6-yl)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecane Alkyl-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)-3,6-二氢吡啶-1(2H)- 羧酸叔丁酯的制备Step 1: 4-(7-Methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl)- Preparation of 3,6-dihydropyridine-1(2H)-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000642
Figure PCTCN2022088560-appb-000642
向4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯(200mg,0.539mmol)在DCM(10mL)溶液中的混合物中加入TPSCl(245mg,0.809mmol)，DMAP(35mg,0.269mmol)和TEA(163mg,1.617mmol)。反应混合物在25℃下搅拌反应过夜。将反应物混合物用DCM稀释，并用碳酸氢钠(饱和水溶液)洗涤。收集有机层，有机层经无水硫酸钠干燥，过滤，并减压浓缩。浓缩物经柱层析纯化得到目标产物。To a solution of tert-butyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)piperidine-1-carboxylate (200 mg, 0.539 mmol) in DCM (10 mL) To the mixture was added TPSCl (245 mg, 0.809 mmol), DMAP (35 mg, 0.269 mmol) and TEA (163 mg, 1.617 mmol). The reaction mixture was stirred at 25°C overnight. The reaction mixture was diluted with DCM and washed with sodium bicarbonate (saturated aqueous solution). The organic layer was collected, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝638.2. LC-MS: (ESI, m/z): [M+H] + = 638.2.
步骤2：(R)-4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯的制备Step 2: (R)-4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinoline Preparation of oxazolin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylic acid tert-butyl ester
Figure PCTCN2022088560-appb-000643
Figure PCTCN2022088560-appb-000643
向4-(7-甲氧基-2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧基)喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯(220mg,0.345mmol)在DCM(5mL)溶液中的混合物中加入(R)-1-(3-硝基-5-(三氟甲基)苯基)乙-1-胺(150mg,0.414mmol)和TEA(105mg,1.035mmol)。反应混合物于90℃下搅拌反应过夜。反应混合物用水淬灭，并用EA萃取。收集有机层，有机层经无水硫酸钠干燥，减压浓缩，浓缩物经柱层析纯化得目标化合物。To 4-(7-methoxy-2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)quinazolin-6-yl)-3, To a mixture of 6-dihydropyridine-1(2H)-carboxylate tert-butyl ester (220 mg, 0.345 mmol) in DCM (5 mL) was added (R)-1-(3-nitro-5-(trifluoro) Methyl)phenyl)ethan-l-amine (150 mg, 0.414 mmol) and TEA (105 mg, 1.035 mmol). The reaction mixture was stirred at 90°C overnight. The reaction mixture was quenched with water and extracted with EA. The organic layer was collected, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the concentrate was purified by column chromatography to obtain the target compound.
LC-MS:(ESI,m/z):[M+H] +＝588.2. LC-MS: (ESI, m/z): [M+H] + = 588.2.
步骤3：(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(1,2,3,6-四氢吡啶-4-基)喹唑啉-4-胺的制备Step 3: (R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(1,2 Preparation of ,3,6-tetrahydropyridin-4-yl)quinazolin-4-amine
Figure PCTCN2022088560-appb-000644
Figure PCTCN2022088560-appb-000644
向(R)-4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯(200mg,0.340mmol)在DCM(4mL)溶液中的混合物中加入三氟乙酸(2mL)。反应混合物于25℃下搅拌1.0小时。将反应混合物用氢氧化钠(40％)水溶液淬灭，并用DCM(50mL×3)萃取。收集有机层，并用无水硫酸钠干燥，减压浓缩，得到目标产物。To (R)-4-(7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline To a mixture of -6-yl)-3,6-dihydropyridine-1(2H)-carboxylate tert-butyl ester (200 mg, 0.340 mmol) in DCM (4 mL) was added trifluoroacetic acid (2 mL). The reaction mixture was stirred at 25°C for 1.0 hour. The reaction mixture was quenched with aqueous sodium hydroxide (40%) and extracted with DCM (50 mL x 3). The organic layer was collected, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝488.2. LC-MS: (ESI, m/z): [M+H] + = 488.2.
步骤4：(R)-4-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-1,2,3,6-四氢吡啶-1-羰基)哌啶-1-甲酸叔丁酯的制备Step 4: (R)-4-(4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Preparation of amino)quinazolin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)piperidine-1-carboxylic acid tert-butyl ester
Figure PCTCN2022088560-appb-000645
Figure PCTCN2022088560-appb-000645
(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(1,2,3,6-四氢吡啶-4-基)喹唑啉-4-胺(10mg,0.017mmol)，1-(叔丁氧基羰基)哌啶-4-羧酸(9mg,0.034mmol)，HATU(10mg,0.025mmol)，DIEA(7mg,0.051mmol)的DMF(1.0mL)反应混合物于25℃下搅拌反应过夜。减压浓缩反应液，浓缩物经柱层析纯化的目标产物。粗产物用于下一步。(R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(1,2,3, 6-Tetrahydropyridin-4-yl)quinazolin-4-amine (10 mg, 0.017 mmol), 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (9 mg, 0.034 mmol), HATU (10 mg) , 0.025 mmol), DIEA (7 mg, 0.051 mmol) in DMF (1.0 mL) reaction mixture was stirred at 25 °C overnight. The reaction solution was concentrated under reduced pressure, and the concentrate was purified by column chromatography to obtain the target product. The crude product was used in the next step.
LC-MS:(ESI,m/z):[M+H] +＝699.4. LC-MS: (ESI, m/z): [M+H] + = 699.4.
步骤5：(R)-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-3,6-二氢吡 啶-1(2H)-基)(哌啶-4-基)甲酮的制备Step 5: (R)-(4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) Preparation of quinazolin-6-yl)-3,6-dihydropyridin-1(2H)-yl)(piperidin-4-yl)methanone
Figure PCTCN2022088560-appb-000646
Figure PCTCN2022088560-appb-000646
向(R)-4-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-1,2,3,6-四氢吡啶-1-羰基)哌啶-1-甲酸叔丁酯(200mg,0.340mmol)在DCM(4mL)溶液中的混合物中加入三氟乙酸(2mL)，反应混合物在25℃下搅拌反应1.0小时后，用NaOH(40％)水溶液淬灭反应，并用DCM(50mL×3)萃取。收集有机层，并用无水硫酸钠干燥，减压浓缩，得到目标产物。To (R)-4-(4-(7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) A mixture of quinazolin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)piperidine-1-carboxylic acid tert-butyl ester (200 mg, 0.340 mmol) in DCM (4 mL) Trifluoroacetic acid (2 mL) was added, and after the reaction mixture was stirred at 25°C for 1.0 h, the reaction was quenched with aqueous NaOH (40%) and extracted with DCM (50 mL x 3). The organic layer was collected, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝599.3. LC-MS: (ESI, m/z): [M+H] + = 599.3.
步骤6：(R)-9-((4-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-1,2,3,6-四氢吡啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯的制备Step 6: (R)-9-((4-(4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl) )ethyl)amino)quinazolin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5] Preparation of undecane-3-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000647
Figure PCTCN2022088560-appb-000647
向(R)-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-基)(哌啶-4-基)甲酮(140.0mg,0.2mmol)和9-甲酰基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(100.0mg,0.36mmol)在THF(6.0mL)溶液中的混合物中缓慢加入STAB(107mg,0.5mmol)。反应混合物在室温下搅拌反应过夜。用水(20.0mL)淬灭反应，并用EA(20.0mL×2)萃取溶液。收集有机相，有机相经无水硫酸钠干燥，并减压浓缩，得到目标粗产物。粗产物用于下一步。To (R)-(4-(7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazole Lin-6-yl)-3,6-dihydropyridin-1(2H)-yl)(piperidin-4-yl)methanone (140.0 mg, 0.2 mmol) and 9-formyl-3-azaspiro [5.5] Undecane-3-carboxylate tert-butyl ester (100.0 mg, 0.36 mmol) in THF (6.0 mL) was slowly added STAB (107 mg, 0.5 mmol). The reaction mixture was stirred at room temperature overnight. The reaction was quenched with water (20.0 mL), and the solution was extracted with EA (20.0 mL x 2). The organic phase was collected, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the target crude product. The crude product was used in the next step.
LC-MS:(ESI,m/z):[M+H] +＝864.5. LC-MS: (ESI, m/z): [M+H] + = 864.5.
步骤7：(R)-9-((4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯的制备Step 7: (R)-9-((4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert. Preparation of butyl esters
Figure PCTCN2022088560-appb-000648
Figure PCTCN2022088560-appb-000648
(R)-9-((4-(4-(7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-1,2,3,6-四氢吡啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯(100.0mg,0.19mmol)和Pd/C(20.0mg)在MeOH(5.0mL)溶液中的混合物在氢气氛围下于室温下搅拌反应过夜。过滤反应液，浓缩滤液，得到目标粗产物。粗产物直接用于下一步反应。(R)-9-((4-(4-(7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) )amino)quinazolin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecane A mixture of -3-carboxylate tert-butyl ester (100.0 mg, 0.19 mmol) and Pd/C (20.0 mg) in MeOH (5.0 mL) was stirred overnight at room temperature under a hydrogen atmosphere. The reaction solution was filtered, and the filtrate was concentrated to obtain the target crude product. The crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝836.7. LC-MS: (ESI, m/z): [M+H] + = 836.7.
步骤8：(R)-(1-((3-氮杂螺并[5.5]十一烷-9-基)甲基)哌啶-4-基)(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-基)甲酮的制备Step 8: (R)-(1-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)(4-(4-((1-( Preparation of 3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)piperidin-1-yl)methanone
Figure PCTCN2022088560-appb-000649
Figure PCTCN2022088560-appb-000649
(R)-9-((4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯(140mg,0.2mmol)在TFA/DCM(3.0mL,1:5)混合溶液中的反应混合物于室温下搅拌反应2.0小时。减压浓缩，得到目标粗产物。粗产物用于下一步。(R)-9-((4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)amino)-7-methoxy- 2-Methylquinazolin-6-yl)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester The reaction mixture (140 mg, 0.2 mmol) in a mixed solution of TFA/DCM (3.0 mL, 1:5) was stirred at room temperature for 2.0 hours. Concentration under reduced pressure gave the target crude product. The crude product was used in the next step.
LC-MS:(ESI,m/z):[M+H] +＝736.7. LC-MS: (ESI, m/z): [M+H] + = 736.7.
步骤9：(R)-1-(5-(9-((4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 9: (R)-1-(5-(9-((4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) Amino)-7-methoxy-2-methylquinazolin-6-yl)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecane Preparation of -3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000650
Figure PCTCN2022088560-appb-000650
向(R)-(1-((3-氮杂螺并[5.5]十一烷-9-基)甲基)哌啶-4-基)(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-基)甲酮(100.0mg,0.14mmol)在DMSO(5.0mL)溶液中的混合物中加入DIEA(54.2mg,0.42mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯基酯(73.0mg,0.17mmol)，反应混合物于室温下搅拌反应3.0h。加入水(15mL)淬灭反应，并用EA(20mL×2)萃取，收集有机层，并用饱和食盐水(20mL)洗涤，无水硫酸钠干燥。浓缩物经制备型HPLC纯化，得到目标产物。To (R)-(1-((3-azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)(4-(4-((1-(3- Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)piperidin-1-yl)methanone (100.0 mg, 0.14 mmol) in DMSO (5.0 mL) was added DIEA (54.2 mg, 0.42 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) Pentafluorophenyl benzoate (73.0 mg, 0.17 mmol), the reaction mixture was stirred at room temperature for 3.0 h. Water (15 mL) was added to quench the reaction, and extracted with EA (20 mL×2). The organic layer was collected, washed with saturated brine (20 mL), and dried over anhydrous sodium sulfate. The concentrate was purified by preparative HPLC to give the desired product.
LC-MS:(ESI,m/z):[M+H] +＝986.4 LC-MS: (ESI, m/z): [M+H] + = 986.4
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.14(d,J＝7.3Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.39(d,J＝8.2Hz,1H),7.02(s,1H),6.87(s,1H),6.84(s,1H),6.69(s,1H),5.62-5.44(m,3H),4.69-4.59(m,1H),4.12-4.01(m,1H),3.90(s,3H),3.82-3.71(m,1H),3.66-3.52(m,3H),3.27-3.10(m,3H),2.86-2.65(m,4H),2.71-2.51(m,2H),2.36(s,3H),2.19-2.04(m,2H),1.93-1.83(m,2H),1.85-7.72(m,2H),1.69-1.42(m,16H),1.41-1.21(m,2H),1.17-0.97(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.14(d, J=7.3Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(s,1H),7.39(d,J=8.2Hz,1H),7.02(s,1H),6.87(s,1H),6.84(s,1H),6.69(s,1H),5.62- 5.44(m,3H),4.69-4.59(m,1H),4.12-4.01(m,1H),3.90(s,3H),3.82-3.71(m,1H),3.66-3.52(m,3H), 3.27-3.10(m, 3H), 2.86-2.65(m, 4H), 2.71-2.51(m, 2H), 2.36(s, 3H), 2.19-2.04(m, 2H), 1.93-1.83(m, 2H ),1.85-7.72(m,2H),1.69-1.42(m,16H),1.41-1.21(m,2H),1.17-0.97(m,4H).
实施例5：(R)-1-(5-(9-((4-(4-((4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 5: (R)-1-(5-(9-((4-(4-((4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(R)-4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧)哌啶-1-羰基)哌啶-1-羧酸叔丁基酯的制备Step 1: (R)-4-(4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) ) Amino)quinazolin-6-yl)oxy)piperidine-1-carbonyl)piperidine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000651
Figure PCTCN2022088560-appb-000651
将(R)-1-(5-(9-((4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮(140mg,0.277mmol)，1-(叔丁氧基羰基)哌啶-4-甲酸(70mg,0.305mmol)，HATU(126mg,0.332mmol)和DIEA(107mg,0.831mmol)在DMF(5mL)溶液中的混合物于室温下搅拌反应过夜。将反应混合物倒入水(50mL)中，搅拌并过滤。干燥滤饼，得到目标产品。粗产物直接用于下一步反应。(R)-1-(5-(9-((4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)amino) -7-Methoxy-2-methylquinazolin-6-yl)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione (140mg, 0.277mmol), 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (70mg, 0.305 mmol), a mixture of HATU (126 mg, 0.332 mmol) and DIEA (107 mg, 0.831 mmol) in DMF (5 mL) was stirred at room temperature overnight. The reaction mixture was poured into water (50 mL), stirred and filtered. The filter cake was dried to obtain the target product. The crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝717.5. LC-MS: (ESI, m/z): [M+H] + = 717.5.
步骤2：(R)-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)(哌啶-4-基)甲酮的制备Step 2: (R)-(4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino ) quinazolin-6-yl)oxy)piperidin-1-yl)(piperidin-4-yl)methanone preparation
Figure PCTCN2022088560-appb-000652
Figure PCTCN2022088560-appb-000652
将(R)-4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧)哌啶-1-羰基)哌啶-1-羧酸叔丁基酯(170mg,粗品)在TFA/DCM(4mL,1:3)溶液中的混合物于室温下搅拌反应1h。减压浓缩反应混合物，得到目标产物。粗产物直接用于下一步。(R)-4-(4-((7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino )quinazolin-6-yl)oxy)piperidine-1-carbonyl)piperidine-1-carboxylate tert-butyl ester (170 mg, crude) in TFA/DCM (4 mL, 1:3) in The reaction was stirred at room temperature for 1 h. The reaction mixture was concentrated under reduced pressure to obtain the desired product. The crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝617.3. LC-MS: (ESI, m/z): [M+H] + = 617.3.
步骤3：(R)-9-((4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯Step 3: (R)-9-((4-(4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)benzene) yl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- tert-butyl carboxylate
Figure PCTCN2022088560-appb-000653
Figure PCTCN2022088560-appb-000653
将(R)-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)(哌啶-4-基)甲酮(180mg,粗品)，9-甲酰基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯(70mg,0.249mmol)和STAB(240mg,1.13mmol)在THF(5mL)溶液中的反应混合物于室温下搅拌反应过夜。用水(50mL)淬灭反应，并用EA(50mL×3)萃取。收集有机层，并用水(100mL×2)和饱和食盐水(100mL)洗涤，用无水硫酸钠干燥，过滤并浓缩。浓缩物经柱层析纯化，得到目标产物。(R)-(4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinoline oxazolin-6-yl)oxy)piperidin-1-yl)(piperidin-4-yl)methanone (180 mg, crude), 9-formyl-3-azaspiro[5.5]undecan- The reaction mixture of tert-butyl 3-carboxylate (70 mg, 0.249 mmol) and STAB (240 mg, 1.13 mmol) in THF (5 mL) was stirred at room temperature overnight. The reaction was quenched with water (50 mL) and extracted with EA (50 mL x 3). The organic layer was collected, washed with water (100 mL×2) and saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The concentrate was purified by column chromatography to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝882.5. LC-MS: (ESI, m/z): [M+H] + = 882.5.
步骤4：(R)-(1-((3-氮杂螺并[5.5]十一烷-9-基)甲基)哌啶-4-基)(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲酮的制备Step 4: (R)-(1-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)(4-((7-methoxy- 2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl ) preparation of ketone
Figure PCTCN2022088560-appb-000654
Figure PCTCN2022088560-appb-000654
将(R)-9-((4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁基酯(182mg,0.206mmol)在DCM(4mL)和TFA(1mL)溶液中的反应混合物于25℃下搅拌反应2h。减压浓缩反应物，得到目标产物。(R)-9-((4-(4-((7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)) ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid The reaction mixture of tert-butyl ester (182 mg, 0.206 mmol) in DCM (4 mL) and TFA (1 mL) was stirred at 25 °C for 2 h. The reaction was concentrated under reduced pressure to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝782.50. LC-MS: (ESI, m/z): [M+H] + =782.50.
步骤5：(R)-1-(2-氯-5-(9-((4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基))苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: (R)-1-(2-Chloro-5-(9-((4-(4-((7-Methoxy-2-methyl-4-((1-(3-nitro -5-(Trifluoromethyl))phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-nitrogen Preparation of heterospiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000655
Figure PCTCN2022088560-appb-000655
向(R)-(1-((3-氮杂螺并[5.5]十一烷-9-基)甲基)哌啶-4-基)(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲酮(145mg,0.19mmol)在DMSO(4.0mL)溶液中的混合物中加入DIEA(0.1mL)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯基酯(9.0mg,0.23mmol)。反应混合物于室温搅拌反应过夜。用水淬灭反应，并用EA萃取。收集有机层，有机层经无水硫酸钠干燥，过滤，并将滤液浓缩，得到目标产物。To (R)-(1-((3-azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)(4-((7-methoxy-2- Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl To a mixture of ketone (145 mg, 0.19 mmol) in DMSO (4.0 mL) was added DIEA (0.1 mL) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) ) pentafluorophenyl benzoate (9.0 mg, 0.23 mmol). The reaction mixture was stirred at room temperature overnight. The reaction was quenched with water and extracted with EA. The organic layer was collected, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to obtain the desired product.
LC-MS:(ESI,m/z):[M-18+H] +＝1031.43. LC-MS: (ESI, m/z): [M-18+H] + = 1031.43.
步骤6：(R)-1-(5-(9-((4-(4-((4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: (R)-1-(5-(9-((4-(4-((4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro[5.5]dec Preparation of monoalkane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000656
Figure PCTCN2022088560-appb-000656
向(R)-1-(2-氯-5-(9-((4-(4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基))苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-羰基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(160mg,0.16mmol)在乙醇/水(3mL/1mL)溶液中的混合物中加入氯化铵(83.0mg,1.55mmol)和铁粉(86.6mg,1.55mmol)。反应混合物在氮氛围下于70℃搅拌反应2小时。反应液用硅藻土过滤，浓缩滤液，浓缩物经制备型HPLC纯化，得到目标产物。To (R)-1-(2-chloro-5-(9-((4-(4-((7-methoxy-2-methyl-4-((1-(3-nitro-5 -(trifluoromethyl))phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-carbonyl)piperidin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (160 mg, 0.16 mmol) in ethanol/water (3 mL/1 mL) was added Ammonium chloride (83.0 mg, 1.55 mmol) and iron powder (86.6 mg, 1.55 mmol). The reaction mixture was stirred at 70°C for 2 hours under nitrogen atmosphere. The reaction solution was filtered through celite, the filtrate was concentrated, and the concentrate was purified by preparative HPLC to obtain the target product.
LC-MS:(ESI,m/z):[M+H] +＝1002.5 LC-MS: (ESI, m/z): [M+H] + = 1002.5
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),7.91(d,J＝7.9Hz,1H),7.85(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.8Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),7.06(s,1H),6.87(s,1H),6.84(s,1H),6.69(s,1H),5.64–5.35(m,3H),4.72–4.64(m,1H),3.87(s,3H),3.81–3.69(m,3H),3.66–3.54(m,3H),3.47–3.39(m,2H),2.89–2.68(m,4H),2.63–2.53(m,1H),2.35(s,3H),2.15–2.03(m,2H),2.00–1.81(m,4H),1.76–1.19(m,20H),1.16–0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 7.91(d, J=7.9Hz, 1H), 7.85(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝1.8Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),7.06(s,1H),6.87(s,1H),6.84(s,1H),6.69( s, 1H), 5.64–5.35 (m, 3H), 4.72–4.64 (m, 1H), 3.87 (s, 3H), 3.81–3.69 (m, 3H), 3.66–3.54 (m, 3H), 3.47– 3.39 (m, 2H), 2.89–2.68 (m, 4H), 2.63–2.53 (m, 1H), 2.35 (s, 3H), 2.15–2.03 (m, 2H), 2.00–1.81 (m, 4H), 1.76–1.19 (m, 20H), 1.16–0.92 (m, 4H).
实施例6：(R)-1-(5-(9-((4-((4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 6: (R)-1-(5-(9-((4-((4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2 -Chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(R)-9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: (R)-9-((4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Preparation of tert-butyl)-amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000657
Figure PCTCN2022088560-appb-000657
将(R)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-氧基)喹唑啉-4-胺(100mg,0.198mmol)，9-甲醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(83mg,0.297mmol)和STAB(210mg,0.99mmol)在THF(5mL)溶液中的混合物于室温下搅拌过夜。反应用水(50mL)淬灭，EA(50mL×3)萃取。有机相用水(100mL×2)洗，饱和食盐水(100mL)洗，Na 2SO 4干燥，过滤并浓缩。所得粗品经flash柱纯化得到目标产物(R)-9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 (R)-7-Methoxy-2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidine-4- oxy)quinazolin-4-amine (100 mg, 0.198 mmol), tert-butyl 9-carbaldehyde-3-azaspiro[5.5]undecan-3-carboxylate (83 mg, 0.297 mmol) and STAB (210 mg , 0.99 mmol) in THF (5 mL) was stirred at room temperature overnight. The reaction was quenched with water (50 mL) and extracted with EA (50 mL×3). The organic phase was washed with water (100 mL×2), saturated brine (100 mL), dried over Na 2 SO 4 , filtered and concentrated. The obtained crude product was purified by flash column to obtain the target product (R)-9-((4-((7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝771.5. LC-MS: (ESI, m/z): [M+H] + =771.5.
步骤2：(R)-6-((1-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-4-基)氧基)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺的制备Step 2: (R)-6-((1-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)oxy)-7-methoxy - Preparation of 2-methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)quinazolin-4-amine
Figure PCTCN2022088560-appb-000658
Figure PCTCN2022088560-appb-000658
将(R)-9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(130mg,0.169mmol)在TFA/DCM(4mL,1:3)中的反应液于室温下搅拌1h。将反应液浓缩。得目标产物(R)-6-((1-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-4-基)氧基)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺。粗产品直接用于下一步反应。(R)-9-((4-((7-methoxy-2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester (130 mg, 0.169 mmol) in The reaction in TFA/DCM (4 mL, 1:3) was stirred at room temperature for 1 h. The reaction solution was concentrated. The target product (R)-6-((1-((3-azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)oxy)-7-methoxy -2-Methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)quinazolin-4-amine. The crude product was used directly in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝671.3. LC-MS: (ESI, m/z): [M+H] + = 671.3.
步骤3：(R)-1-(2-氯-5-(9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: (R)-1-(2-Chloro-5-(9-((4-((7-Methoxy-2-methyl-4-((1-(3-nitro-5- (Trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- Preparation of carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000659
Figure PCTCN2022088560-appb-000659
将(R)-6-((1-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-4-基)氧基)-7-甲氧基-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)喹唑啉-4-胺(130mg,粗品)，4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(75mg,0.170mmol)和DIEA(110mg,0.85mmol)在DMSO(5mL)中的反应液于室温下搅拌过夜。将反应液倒入水(50mL)中，搅拌，过滤。滤饼真空干燥得目标产物(R)-1-(2-氯-5-(9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。粗产品直接用于下一步反应。(R)-6-((1-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperidin-4-yl)oxy)-7-methoxy-2 -methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)quinazolin-4-amine (130 mg, crude), 4-chloro-3-(2 ,4-dioxotetrahydropyrimidin-1(2H)-yl)pentafluorophenyl benzoate (75 mg, 0.170 mmol) and DIEA (110 mg, 0.85 mmol) in DMSO (5 mL) at room temperature Stir overnight. The reaction solution was poured into water (50 mL), stirred, and filtered. The filter cake was vacuum-dried to obtain the target product (R)-1-(2-chloro-5-(9-((4-((7-methoxy-2-methyl-4-((1-(3-nitro yl)-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecane Alkyl-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione. The crude product was used directly in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝921.4. LC-MS: (ESI, m/z): [M+H] + = 921.4.
步骤4：(R)-1-(5-(9-((4-((4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: (R)-1-(5-(9-((4-((4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2- Preparation of Chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000660
Figure PCTCN2022088560-appb-000660
将(R)-1-(2-氯-5-(9-((4-((7-甲氧基-2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(120mg,0.130mmol)，Fe粉(73mg,1.30mmol)和NH 4Cl(70mg,1.30mmol)在EtOH/H 2O(8mL,3:1)中的反应液于室温下搅拌反应1h。将反应液过滤并浓缩，所得粗品经制备HPLC纯化得到目标产物(R)-1-(5-(9-((4-((4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧基)哌啶-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (R)-1-(2-Chloro-5-(9-((4-((7-methoxy-2-methyl-4-((1-(3-nitro-5-(tri Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl) Phenyl)dihydropyrimidine-2,4(1H,3H)-dione (120 mg, 0.130 mmol), Fe powder (73 mg, 1.30 mmol) and NH 4 Cl (70 mg, 1.30 mmol) in EtOH/H 2 O ( The reaction solution in 8 mL, 3:1) was stirred at room temperature for 1 h. The reaction solution was filtered and concentrated, and the obtained crude product was purified by preparative HPLC to obtain the target product (R)-1-(5-(9-((4-((4-((1-(3-amino-5-(trifluoro) Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxy)piperidin-1-yl)methyl)-3-azaspiro[ 5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝891.4. LC-MS: (ESI, m/z): [M+H] + = 891.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),7.91(d,J＝7.8Hz,1H),7.78(s,1H),7.63(d,J＝8.2Hz,1H),7.55(d,J＝1.8Hz,1H),7.39(dd,J＝8.3,1.8Hz,1H),7.04(s,1H),6.87(s,1H),6.83(s,1H),6.69(s,1H),5.61–5.50(m,3H),4.450–4.42(m,1H),3.86(s,3H),3.80–3.70(m,1H),3.67–3.52(m,3H),2.78–2.61(m,4H),2.35(s,3H),2.30–2.10(m,4H),1.99–1.90(m,2H),1.75–1.65(m,4H),1.60–0.94(m,16H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s,1H),7.91(d,J=7.8Hz,1H),7.78(s,1H),7.63(d,J=8.2Hz,1H) ,7.55(d,J＝1.8Hz,1H),7.39(dd,J＝8.3,1.8Hz,1H),7.04(s,1H),6.87(s,1H),6.83(s,1H),6.69( s, 1H), 5.61–5.50 (m, 3H), 4.450–4.42 (m, 1H), 3.86 (s, 3H), 3.80–3.70 (m, 1H), 3.67–3.52 (m, 3H), 2.78– 2.61 (m, 4H), 2.35 (s, 3H), 2.30–2.10 (m, 4H), 1.99–1.90 (m, 2H), 1.75–1.65 (m, 4H), 1.60–0.94 (m, 16H).
实施例7：1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 7: 1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-di Azaspiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-((1-((苄氧基)羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: tert-butyl 9-((1-((benzyloxy)carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]undecan-3-carboxylate preparation
Figure PCTCN2022088560-appb-000661
Figure PCTCN2022088560-appb-000661
向3,9-二氮杂螺[5.5]十一烷-3-羧酸酯(300.0mg,1.2mmol)和苯基4-甲醛哌啶-1-羧酸叔丁酯(346.0mg,1.4mmol)的THF(5mL)溶液中缓慢加入STAB(770.0mg,3.6mmol)，反应液于室温下搅拌过夜。反应用水(20mL)淬灭，EA(50mL×2)萃取。有机相饱和NaHCO 3溶液洗，Na 2SO 4干燥，过滤并浓缩。所得粗品经硅胶柱层析(EtOAc-PE,0-30％)纯化得到目标产物9-((1-((苄氧基)羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To 3,9-diazaspiro[5.5]undecan-3-carboxylate (300.0 mg, 1.2 mmol) and phenyl 4-carbaldehyde piperidine-1-carboxylate tert-butyl ester (346.0 mg, 1.4 mmol) ) in THF (5 mL) was slowly added STAB (770.0 mg, 3.6 mmol), and the reaction solution was stirred at room temperature overnight. The reaction was quenched with water (20 mL) and extracted with EA (50 mL×2). The organic phase was washed with saturated NaHCO3 solution, dried over Na2SO4 , filtered and concentrated. The obtained crude product was purified by silica gel column chromatography (EtOAc-PE, 0-30%) to obtain the target product 9-((1-((benzyloxy)carbonyl)piperidin-4-yl)methyl)-3,9- Diazaspiro[5.5]undecane-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝486.4. LC-MS: (ESI, m/z): [M+H] + = 486.4.
步骤2：9-(哌啶-4-基甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-(piperidin-4-ylmethyl)-3,9-diazaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000662
Figure PCTCN2022088560-appb-000662
将9-((1-((苄氧基)羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯(300.0mg,0.6mmol)和10％Pd/C(60.0mg)在EtOAc(5mL)中的反应液在70℃下H 2(60psi)氛围下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-(哌啶-4-基甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步。 9-((1-((benzyloxy)carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]undecan-3-carboxylate tert-butyl ester (300.0 mg, 0.6 mmol) and 10% Pd/C (60.0 mg) in EtOAc (5 mL) was stirred overnight at 70 °C under an atmosphere of H2 (60 psi). The reaction solution was filtered through celite and concentrated to obtain the target product 9-(piperidin-4-ylmethyl)-3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The resulting crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝352.4. LC-MS: (ESI, m/z): [M+H] + = 352.4.
步骤3：9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tris) Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5] Preparation of tert-butyl undecane-3-carboxylate
Figure PCTCN2022088560-appb-000663
Figure PCTCN2022088560-appb-000663
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基-1-羧酸(140.0mg,0.2mmol)，9-(哌啶-4-基甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯(84.0mg,0.24mmol)和HATU(114mg,0.3mmol)的DMF(2.0mL)溶液中缓慢滴加DIEA(78.0mg,0.6mmol)。反应液在室温下搅拌反应2h。反应液用冰水淬灭(20mL)，过滤，滤饼经真空干燥得目标产物9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexyl-1-carboxylic acid (140.0 mg, 0.2 mmol), 9-(piperidin-4-ylmethyl)-3,9-diazaspiro[5.5] To a solution of tert-butyl undecane-3-carboxylate (84.0 mg, 0.24 mmol) and HATU (114 mg, 0.3 mmol) in DMF (2.0 mL) was slowly added DIEA (78.0 mg, 0.6 mmol) dropwise. The reaction solution was stirred at room temperature for 2 h. The reaction solution was quenched with ice water (20 mL), filtered, and the filter cake was dried under vacuum to obtain the target product 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4- (((R)-1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidine-4 -yl)methyl)-3,9-diazaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The resulting crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝866.5. LC-MS: (ESI, m/z): [M+H] + = 866.5.
步骤4：9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 4: 9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]dec Preparation of tert-butyl monoalkane-3-carboxylate
Figure PCTCN2022088560-appb-000664
Figure PCTCN2022088560-appb-000664
将9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯(130.0mg,0.15mmol)和10％Pd/C(30.0mg)在MeOH(10.0mL)中的反应液在70℃下H 2(90psi)氛围下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步反应。 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4-((((R)-1-(3-nitro-5-(trifluoromethyl) yl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]undecyl A reaction of tert-butyl alkane-3-carboxylate (130.0 mg, 0.15 mmol) and 10% Pd/C (30.0 mg) in MeOH (10.0 mL) was stirred overnight at 70 °C under an atmosphere of H2 (90 psi). The reaction solution was filtered through celite and concentrated to obtain the target product 9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9 - tert-butyl diazaspiro[5.5]undecane-3-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝836.5. LC-MS: (ESI, m/z): [M+H] + = 836.5.
步骤5：(4-((3,9-二氮杂螺[5.5]十一烷-3-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮的制备Step 5: (4-((3,9-diazaspiro[5.5]undecan-3-yl)methyl)piperidin-1-yl)((1R,4R)-4-(4-( ((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl) Preparation of ketone
Figure PCTCN2022088560-appb-000665
Figure PCTCN2022088560-appb-000665
将9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羧酸叔丁酯(90.0mg,0.1mmol)在TFA/DCM(1.0mL/3.0mL)中的反应液在室温下搅拌反应1h。反应液直接浓缩得目标产物(4-((3,9-二氮杂螺[5.5]十一烷-3-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮。所得粗品直接用于下一步反应。9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]undecane The reaction solution of -3-carboxylate tert-butyl ester (90.0 mg, 0.1 mmol) in TFA/DCM (1.0 mL/3.0 mL) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain the target product (4-((3,9-diazaspiro[5.5]undecan-3-yl)methyl)piperidin-1-yl)((1R,4R)-4- (4-(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl ) cyclohexane) ketone. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝736.4. LC-MS: (ESI, m/z): [M+H] + = 736.4.
步骤6：1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉 -6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Step 6: 1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3,9-diazo Heterospiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000666
Figure PCTCN2022088560-appb-000666
向(4-((3,9-二氮杂螺[5.5]十一烷-3-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮(100.0mg,0.12mmol)的DMSO(5.0mL)溶液中加入DIEA(54.20mg,0.42mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(73.0mg,0.17mmol)，反应液在室温下搅拌2h。反应液加水(15.0mL)，用EA(20mL×2)萃取。有机相用饱和食盐水(20mL)洗，无水Na 2SO 4干燥，浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得目标产物1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3,9-二氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (4-((3,9-diazaspiro[5.5]undecan-3-yl)methyl)piperidin-1-yl)((1R,4R)-4-(4-(((( R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane)methane To a solution of ketone (100.0 mg, 0.12 mmol) in DMSO (5.0 mL) was added DIEA (54.20 mg, 0.42 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)- base) pentafluorophenyl benzoate (73.0 mg, 0.17 mmol), the reaction solution was stirred at room temperature for 2 h. The reaction solution was added with water (15.0 mL) and extracted with EA (20 mL×2). The organic phase was washed with saturated brine (20 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(5-(9-((1-((1R,4R)-4-(4-( ((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane -1-Carbonyl)piperidin-4-yl)methyl)-3,9-diazaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4( 1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝986.4. LC-MS: (ESI, m/z): [M+H] + = 986.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.16-8.02(m,2H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.38(d,J＝8.2Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65-5.47(m,3H),4.41-4.38(m,1H),3.89-3.75(m,4H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.31-2.90(m,2H),2.78-2.72(m,2H),2.70-2.60(m,1H),2.55-2.51(m,1H),2.45-2.20(m,7H),2.15-2.05(m,2H),1.95-1.29(m,24H),1.17-0.98(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s,1H),8.16-8.02(m,2H),7.63(d,J=8.2Hz,1H),7.54(s,1H),7.38( d, J＝8.2Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65-5.47(m, 3H), 4.41-4.38 (m,1H),3.89-3.75(m,4H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.31-2.90(m,2H),2.78-2.72(m,2H) ,2.70-2.60(m,1H),2.55-2.51(m,1H),2.45-2.20(m,7H),2.15-2.05(m,2H),1.95-1.29(m,24H),1.17-0.98( m, 2H).
实施例8：1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 8: 1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-(羟基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 9-(hydroxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000667
Figure PCTCN2022088560-appb-000667
在-78℃时向n-BuLi(2.3mL,2.5M/正己烷,5.7mmol)的无水THF(15mL)溶液中滴加4-溴吡啶(1.0g,6.3mmol)的无水THF(5.0mL)溶液，在-78℃条件下搅拌15min后，再缓慢滴加9-甲醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.5g,5.3mmol)的THF溶液。反应液在-78℃条件下继续搅拌45min。在-70℃下反应用水(20mL)淬灭，EA(20mL×2)萃取。有机相用饱和食盐水洗，Na 2SO 4干燥，过滤并浓缩。所得粗品经硅胶柱层析(EtOAc-PE,0-30％)纯化得目标产物9-(羟基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a solution of n-BuLi (2.3 mL, 2.5 M/n-hexane, 5.7 mmol) in dry THF (15 mL) at -78 °C was added dropwise 4-bromopyridine (1.0 g, 6.3 mmol) in dry THF (5.0 mL) solution, stirred at -78 °C for 15 min, and then slowly added dropwise 9-carbaldehyde-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (1.5 g, 5.3 mmol) in THF solution. The reaction solution was stirred for 45 min at -78°C. The reaction was quenched with water (20 mL) at -70°C and extracted with EA (20 mL×2). The organic phase was washed with saturated brine, dried over Na2SO4 , filtered and concentrated. The obtained crude product was purified by silica gel column chromatography (EtOAc-PE, 0-30%) to obtain the target product 9-(hydroxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecan-3- tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝361.1. LC-MS: (ESI, m/z): [M+H] + = 361.1.
步骤2：9-(乙酰氧基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-(acetoxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000668
Figure PCTCN2022088560-appb-000668
将9-(羟基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.0g,2.7mmol)，Ac 2O(0.4g,4.0mol)和TEA(0.2ml)在DCE(10.0mL)中的反应液在70℃条件下搅拌5h。反应液浓缩，然后用氯仿萃取，有机相浓缩。所得粗品经硅胶柱层析纯化得目标产物9-(乙酰氧基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 9-(Hydroxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (1.0 g, 2.7 mmol), Ac 2 O (0.4 g, 4.0 mol) and TEA (0.2 ml) in DCE (10.0 mL) were stirred at 70 °C for 5 h. The reaction solution was concentrated, then extracted with chloroform, and the organic phase was concentrated. The obtained crude product was purified by silica gel column chromatography to obtain the target product 9-(acetoxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝403.2. LC-MS: (ESI, m/z): [M+H] + = 403.2.
步骤3：9-(吡啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 9-(pyridin-4-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000669
Figure PCTCN2022088560-appb-000669
将9-(乙酰氧基(吡啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(600.0mg,1.5mmol)，10％Pd/C (150.0mg)和甲酸铵(472.0mg,7.5mmol)在MeOH(10.0mL)中的反应液在80℃下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-(吡啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗产品直接用于下一步反应。9-(Acetoxy(pyridin-4-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (600.0 mg, 1.5 mmol), 10% Pd/C (150.0 mg) and ammonium formate (472.0 mg, 7.5 mmol) in MeOH (10.0 mL) was stirred at 80 °C overnight. The reaction solution was filtered through celite and concentrated to obtain the target product 9-(pyridin-4-ylmethyl)-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝345.2. LC-MS: (ESI, m/z): [M+H] + = 345.2.
步骤4：9-(哌啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 9-(piperidin-4-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000670
Figure PCTCN2022088560-appb-000670
将9-(吡啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(450.0mg,1.3mmol)，10％Pd/C(80.0mg)在i-PrOH(10.0mL)和H 2O(5.0mL)中的反应液在70℃下H 2(90psi)氛围下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-(哌啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗产品直接用于下一步反应。 9-(Pyridin-4-ylmethyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (450.0 mg, 1.3 mmol), 10% Pd/C (80.0 mg) in The reaction in i-PrOH (10.0 mL) and H2O (5.0 mL) was stirred overnight at 70°C under an atmosphere of H2 (90 psi). The reaction solution was filtered through celite and concentrated to obtain the target product 9-(piperidin-4-ylmethyl)-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝351.1. LC-MS: (ESI, m/z): [M+H] + = 351.1.
步骤5：9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷3-羧酸叔丁酯的制备Step 5: 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tris) Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro[5.5]undecane Preparation of tert-butyl 3-carboxylate
Figure PCTCN2022088560-appb-000671
Figure PCTCN2022088560-appb-000671
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基-1-羧酸(140.0mg,0.2mmol)，9-(哌啶-4-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(84.0mg,0.24mmol)和HATU(114mg,0.3mmol)的DMF(2.0mL)溶液中缓慢滴加DIEA(78.0mg,0.6mmol)，然后反应液在室温搅拌2h。反应用冰水(20mL)淬灭，过滤，滤饼真空干燥得目标产物9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷3-羧酸叔丁酯。所得粗产品直接用于下一步反应。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexyl-1-carboxylic acid (140.0 mg, 0.2 mmol), 9-(piperidin-4-ylmethyl)-3-azaspiro[5.5]undecane DIEA (78.0 mg, 0.6 mmol) was slowly added dropwise to a solution of tert-butyl-3-carboxylate (84.0 mg, 0.24 mmol) and HATU (114 mg, 0.3 mmol) in DMF (2.0 mL), and then the reaction solution was stirred at room temperature for 2 h . The reaction was quenched with ice water (20 mL), filtered, and the filter cake was vacuum dried to obtain the target product 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4-(( (R)-1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl )methyl)-3-azaspiro[5.5]undecane 3-carboxylate tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝865.4. LC-MS: (ESI, m/z): [M+H] + = 865.4.
步骤6：9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷3-羧酸叔丁酯的制备Step 6: 9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro[5.5]undecane 3 - Preparation of tert-butyl carboxylate
Figure PCTCN2022088560-appb-000672
Figure PCTCN2022088560-appb-000672
将9-((1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷3-羧酸叔丁酯(130.0mg,0.15mmol)和10％Pd/C(30.0mg)在MeOH(10.0mL)中的反应液在70℃下H 2(90psi)氛围下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步反应。 9-((1-((1R,4R)-4-(7-methoxy-2-methyl-4-((((R)-1-(3-nitro-5-(trifluoromethyl) yl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro[5.5]undecane 3- A reaction of tert-butyl carboxylate (130.0 mg, 0.15 mmol) and 10% Pd/C (30.0 mg) in MeOH (10.0 mL) was stirred overnight at 70 °C under an atmosphere of H2 (90 psi). The reaction solution was filtered through celite and concentrated to obtain the target product 9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-nitrogen Heteraspiro[5.5]undecane-3-carboxylate tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝835.5. LC-MS: (ESI, m/z): [M+H] + = 835.5.
步骤7：(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮的制备Step 7: (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperidin-1-yl)((1R,4R)-4-(4-((((R )-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone preparation
Figure PCTCN2022088560-appb-000673
Figure PCTCN2022088560-appb-000673
将9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己 烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷3-羧酸叔丁酯(130.0mg,0.15mmol)在TFA/DCM(3.0mL,1:5)中的反应液在室温下搅拌1h。反应液直接浓缩得产物(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮。所得粗品直接用于下一步反应。9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro[5.5]undecane 3-carboxy The reaction of tert-butyl acid (130.0 mg, 0.15 mmol) in TFA/DCM (3.0 mL, 1:5) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain the product (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperidin-1-yl)((1R,4R)-4-(4-( ((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane ) ketone. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝736.4. LC-MS: (ESI, m/z): [M+H] + = 736.4.
步骤8：1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Step 8: 1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methyl)-3-azaspiro[ 5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000674
Figure PCTCN2022088560-appb-000674
向(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌啶-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮(100.0mg,0.14mmol)的DMSO(5.0mL)溶液中加入DIEA(54.20mg,0.42mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(73.0mg,0.17mmol)，反应液在室温下搅拌2h。反应加水(15mL)淬灭，用EA(20mL×2)萃取，有机相用饱和食盐水(20mL)洗，无水Na 2SO 4干燥，浓缩，粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得目标产物1-(5-(9-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperidin-1-yl)((1R,4R)-4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane)methanone (100.0 mg, 0.14 mmol) in DMSO (5.0 mL) was added DIEA (54.20 mg, 0.42 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzene Pentafluorophenyl formate (73.0 mg, 0.17 mmol), the reaction solution was stirred at room temperature for 2 h. The reaction was quenched by adding water (15 mL), extracted with EA (20 mL×2), the organic phase was washed with saturated brine (20 mL), dried over anhydrous Na 2 SO 4 , concentrated, and the crude product was subjected to preparative HPLC (acetonitrile/0.05% NH 4 HCO) 3 Aqueous solution, 5% to 95%) purified to obtain the target product 1-(5-(9-((1-((1R,4R)-4-(4-((((R)-1-(3-amino- 5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl) Methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝985.4. LC-MS: (ESI, m/z): [M+H] + = 985.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.16-8.02(m,2H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.38(d,J＝8.2Hz,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.65-5.47(m,3H),4.41-4.38(m,1H),3.89-3.75(m,4H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.31-2.90(m,2H),2.78-2.72(m,2H),2.70-2.60(m,1H),2.38-2.35(s,3H),1.86-1.75(m,4H),1.73-1.28(m,22H),1.20-0.95(m,8H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s,1H),8.16-8.02(m,2H),7.63(d,J=8.2Hz,1H),7.54(s,1H),7.38( d, J＝8.2Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.65-5.47(m, 3H), 4.41-4.38 (m,1H),3.89-3.75(m,4H),3.79-3.71(m,1H),3.67-3.54(m,3H),3.31-2.90(m,2H),2.78-2.72(m,2H) ,2.70-2.60(m,1H),2.38-2.35(s,3H),1.86-1.75(m,4H),1.73-1.28(m,22H),1.20-0.95(m,8H).
实施例9：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-((3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)-N-甲基环己烷-1-甲酰胺Example 9: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)-N-((3-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl) )-3-Azaspiro[5.5]undecan-9-yl)methyl)-N-methylcyclohexane-1-carboxamide
步骤1：9-((苯甲基(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 9-((benzyl(methyl)amino)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000675
Figure PCTCN2022088560-appb-000675
向9-甲醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(300.0mg,1.1mmol)和N-甲基-1-苄氨(130.0mg,1.1mmol)的THF(10.0mL)溶液中加入STAB(680.0mg,3.3mmol)，反应液于室温下搅拌过夜。反应液倒入NaHCO 3(20mL)水溶液中，用EA(20mL×2)萃取，有机相用水洗，饱和食盐水洗，Na 2SO 4干燥，过滤并浓缩。所得粗品经硅胶柱层析(EtOAc-PE,0-30％)纯化得目标产物9-((苯甲基(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To tert-butyl 9-carbaldehyde-3-azaspiro[5.5]undecan-3-carboxylate (300.0 mg, 1.1 mmol) and N-methyl-1-benzylamine (130.0 mg, 1.1 mmol) in THF (10.0 mL) STAB (680.0 mg, 3.3 mmol) was added to the solution, and the reaction solution was stirred at room temperature overnight. The reaction solution was poured into aqueous NaHCO 3 (20 mL), extracted with EA (20 mL×2), the organic phase was washed with water, washed with saturated brine, dried over Na 2 SO 4 , filtered and concentrated. The obtained crude product was purified by silica gel column chromatography (EtOAc-PE, 0-30%) to obtain the target product 9-((benzyl(methyl)amino)methyl)-3-azaspiro[5.5]undecan- 3-Carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝387.2. LC-MS: (ESI, m/z): [M+H] + = 387.2.
步骤2：9-((甲基氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-((methylamino)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000676
Figure PCTCN2022088560-appb-000676
将9-((苯甲基(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(240.0mg,0.6mmol)和10％Pd/C(50.0mg)在MeOH(10.0mL)中的反应液于50℃下H 2(60psi)氛围下搅拌过夜。反应液经硅藻土过滤，浓缩得目标产物9-((甲基氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步反应。 9-((Benzyl(methyl)amino)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (240.0 mg, 0.6 mmol) and 10% Pd/C (50.0 mg) The reaction in MeOH (10.0 mL) was stirred overnight at 50 °C under an atmosphere of H2 (60 psi). The reaction solution was filtered through celite and concentrated to obtain the target product 9-((methylamino)methyl)-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝297.2. LC-MS: (ESI, m/z): [M+H] + = 297.2.
步骤3：9-(((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: 9-(((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl) )phenyl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[5.5]undecan-3-carboxy Preparation of tert-butyl acid
Figure PCTCN2022088560-appb-000677
Figure PCTCN2022088560-appb-000677
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基-1-羧酸(120.0mg,0.2mmol),9-((甲氨)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(65.0mg,0.22mmol)和HATU(98.8mg,0.26mmol)的DMF(2.0mL)溶液中缓慢滴加DIEA(78.0mg,0.6mmol)。反应液在室温搅拌2h。反应用冰水(20mL)淬灭，搅拌并过滤。滤饼真空干燥得目标产物9-(((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步反应。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl )amino)quinazolin-6-yl)cyclohexyl-1-carboxylic acid (120.0 mg, 0.2 mmol), 9-((methylamino)methyl)-3-azaspiro[5.5]undecan-3 - To a solution of tert-butyl carboxylate (65.0 mg, 0.22 mmol) and HATU (98.8 mg, 0.26 mmol) in DMF (2.0 mL) was slowly added DIEA (78.0 mg, 0.6 mmol) dropwise. The reaction solution was stirred at room temperature for 2 h. The reaction was quenched with ice water (20 mL), stirred and filtered. The filter cake was vacuum dried to obtain the target product 9-(((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-( Trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[5.5]undecane - tert-butyl 3-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝811.5. LC-MS: (ESI, m/z): [M+H] + = 811.5.
步骤4：9-(((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 4: 9-(((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid Preparation of tert-butyl ester
Figure PCTCN2022088560-appb-000678
Figure PCTCN2022088560-appb-000678
将9-(((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(130.0mg,0.15mmol)和10％Pd/C(30.0mg)在MeOH(10.0mL)中的反应液于70℃下H 2(90psi)氛围下搅拌过夜。反应液经硅藻土过滤，滤液浓缩得目标产物9-(((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。所得粗品直接用于下一步反应。 9-(((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)benzene (yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert. The reaction of butyl ester (130.0 mg, 0.15 mmol) and 10% Pd/C (30.0 mg) in MeOH (10.0 mL) was stirred overnight at 70 °C under an atmosphere of H2 (90 psi). The reaction solution was filtered through celite, and the filtrate was concentrated to obtain the target product 9-(((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[ 5.5] tert-Butyl undecane-3-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝781.5. LC-MS: (ESI, m/z): [M+H] + = 781.5.
步骤5：(1R,4R)-N-((3-氮杂螺[5.5]十一烷-9-基)甲基)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺的制备Step 5: (1R,4R)-N-((3-azaspiro[5.5]undecan-9-yl)methyl)-4-(4-(((R)-1-(3-amino) -5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-carboxamide preparation
Figure PCTCN2022088560-appb-000679
Figure PCTCN2022088560-appb-000679
将9-(((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(100.0mg,0.1mmol)在TFA/DCM(1.0mL/3.0mL)的反应液于室温下搅拌1h。反应液直接浓缩得目标产物(1R,4R)-N-((3-氮杂螺[5.5]十一烷-9-基)甲基)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺。所得粗品直接用于下一步反应。9-(((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy tert-butyl-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-amido)methyl)-3-azaspiro[5.5]undecan-3-carboxylate The reaction of the ester (100.0 mg, 0.1 mmol) in TFA/DCM (1.0 mL/3.0 mL) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain the target product (1R,4R)-N-((3-azaspiro[5.5]undecan-9-yl)methyl)-4-(4-(((R)-1- (3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1 - Formamide. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝681.3. LC-MS: (ESI, m/z): [M+H] + = 681.3.
步骤6：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-((3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)-N-甲基环己烷-1-甲酰胺的制备Step 6: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)-N-((3-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl) - Preparation of 3-azaspiro[5.5]undecan-9-yl)methyl)-N-methylcyclohexane-1-carboxamide
Figure PCTCN2022088560-appb-000680
Figure PCTCN2022088560-appb-000680
向(1R,4R)-N-((3-氮杂螺[5.5]十一烷-9-基)甲基)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺(90.0mg,0.13mmol)的DMSO(5.0mL)溶液中加入DIEA(54.2mg,0.42mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(63.0mg,0.17mmol)，反应液于室温下搅拌反应2h。反应用水(15mL)淬灭，EA(30mL×2)萃取，有机相用饱和食盐水洗，无水Na 2SO 4干燥，浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化，然后再用制备TLC(5.0％MeOH/DCM)纯化得目标产物(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-((3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)-N-甲基环己烷-1-甲酰胺。 To (1R,4R)-N-((3-azaspiro[5.5]undecan-9-yl)methyl)-4-(4-(((R)-1-(3-amino-5 -(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-carboxamide (90.0 mg , 0.13 mmol) in DMSO (5.0 mL) was added DIEA (54.2 mg, 0.42 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid Pentafluorophenyl ester (63.0 mg, 0.17 mmol), the reaction solution was stirred at room temperature for 2 h. The reaction was quenched with water (15 mL), extracted with EA (30 mL×2), the organic phase was washed with saturated brine, dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) followed by preparative TLC (5.0% MeOH/DCM) to give the title product (1R,4R)-4-(4- (((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N -((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9 -yl)methyl)-N-methylcyclohexane-1-carboxamide.
LC-MS:(ESI,m/z):[M+H] +＝931.6. LC-MS: (ESI, m/z): [M+H] + = 931.6.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.15(d,J＝7.6Hz,1H),8.05(d,J＝11.2Hz,1H),7.63(d,J＝8.2Hz,1H),7.55(s,1H),7.38(d,J＝8.3Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65–5.47(m,3H),3.89(s,3H),3.80–3.70(m,1H),3.65–3.51(m,3H),3.25–3.15(s,2H),3.02(s,2H),2.94(d,J＝10.9Hz,1H),2.80(s,1H),2.76–2.69(m,2H),2.68–2.62(m,1H),2.36(s,3H),1.92–1.82(m,3H),1.76–1.51(m,11H),1.45–1.33(m,4H),1.32–1.20(m,4H),1.15–1.02(s,4H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.15 (d, J=7.6 Hz, 1H), 8.05 (d, J=11.2 Hz, 1H), 7.63 (d, J= 8.2Hz, 1H), 7.55(s, 1H), 7.38(d, J=8.3Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65–5.47(m, 3H), 3.89(s, 3H), 3.80–3.70(m, 1H), 3.65–3.51(m, 3H), 3.25–3.15(s, 2H), 3.02(s, 2H), 2.94(d, J=10.9Hz, 1H), 2.80(s, 1H), 2.76-2.69(m, 2H), 2.68-2.62(m, 1H), 2.36(s, 3H), 1.92-1.82 (m, 3H), 1.76–1.51 (m, 11H), 1.45–1.33 (m, 4H), 1.32–1.20 (m, 4H), 1.15–1.02 (s, 4H).
实施例10：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 10: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2 ,3-Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine -1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-溴苯并[b]噻吩1,1-二氧代的制备Step 1: Preparation of 4-bromobenzo[b]thiophene 1,1-dioxo
Figure PCTCN2022088560-appb-000681
Figure PCTCN2022088560-appb-000681
向4-溴苯并[b]噻吩(3.0g,14.2mmol)的DCM(60.0ml)溶液中加入m-CPBA(4.8g,28.4mmol)，反应液于25℃下搅拌反应过夜。反应用冰水(150mL)淬灭，EA(80mL×3)萃取，合并有机相，用食盐水(30mL)洗，有机相经无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝60/40)纯化得目标产物4-溴苯并[b]噻吩1,1-二氧代。 To a solution of 4-bromobenzo[b]thiophene (3.0 g, 14.2 mmol) in DCM (60.0 ml) was added m-CPBA (4.8 g, 28.4 mmol), and the reaction solution was stirred at 25° C. overnight. The reaction was quenched with ice water (150 mL), extracted with EA (80 mL×3), the organic phases were combined, washed with brine (30 mL), the organic phase was dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=60/40) to obtain the target product 4-bromobenzo[b]thiophene 1,1-dioxo.
LC-MS:(ESI,m/z):[M+H] +＝245.1. LC-MS: (ESI, m/z): [M+H] + = 245.1.
步骤2：4-溴-2,3-二氢苯并[b]噻吩1,1-二氧代的制备Step 2: Preparation of 4-bromo-2,3-dihydrobenzo[b]thiophene 1,1-dioxo
Figure PCTCN2022088560-appb-000682
Figure PCTCN2022088560-appb-000682
0℃时向4-溴苯并[b]噻吩1,1-二氧代(4.0g,16.3mmol)的MeOH(40.0ml)溶液中加入NaBH 4(465.3mg,12.2mmol)，反应液于25℃下搅拌反应4.0h。反应用水(100mL)淬灭，EA(80mL×3)萃取，合并有机相，用食盐水(30mL)洗，有机相经无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝70/30)纯化得目标产物4-溴-2,3-二氢苯并[b]噻吩1,1-二氧代。 To a solution of 4-bromobenzo[b]thiophene 1,1-dioxo (4.0 g, 16.3 mmol) in MeOH (40.0 ml) was added NaBH 4 (465.3 mg, 12.2 mmol) at 0 °C, and the reaction solution was added at 25 The reaction was stirred at °C for 4.0 h. The reaction was quenched with water (100 mL), extracted with EA (80 mL×3), the organic phases were combined, washed with brine (30 mL), the organic phase was dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=70/30) to obtain the target product 4-bromo-2,3-dihydrobenzo[b]thiophene 1,1-dioxo.
LC-MS:(ESI,m/z):[M+H] +＝247.1. LC-MS: (ESI, m/z): [M+H] + = 247.1.
步骤3：1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙酮的制备Step 3: Preparation of 1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethanone
Figure PCTCN2022088560-appb-000683
Figure PCTCN2022088560-appb-000683
将4-溴-2,3-二氢苯并[b]噻吩1,1-二氧代(4.0g,16.3mmol)，Pd(PPh 3) 2Cl 2(117.7mg,1.6mmol)，TEA(4.9g,48.9mmol)和三丁基(1-乙氧基乙烯)锡烷(8.8g,24.4mmol)在1,4-二氧六环(80.0mL)中的反应液用N 2置换3次，反应液于80℃下N 2氛围下搅拌反应16.0h。反应用冰水(200mL)淬灭，EA(80mL×3)萃取，合并有机相，用食盐水(50mL)洗，有机相经无水Na 2SO 4干燥，浓缩。粗品在6N HCl(10mL)中室温下搅拌2h，然后浓缩，粗品经柱层析(EA/PE＝30/70)纯化得目标产物1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙酮。 4-Bromo-2,3-dihydrobenzo[b]thiophene 1,1-dioxo (4.0 g, 16.3 mmol), Pd(PPh 3 ) 2 Cl 2 (117.7 mg, 1.6 mmol), TEA ( 4.9 g, 48.9 mmol) and tributyl(1-ethoxyethylene)stannane (8.8 g, 24.4 mmol) in 1,4-dioxane (80.0 mL) were replaced with N 3 times , the reaction solution was stirred at 80 °C under N 2 atmosphere for 16.0 h. The reaction was quenched with ice water (200 mL), extracted with EA (80 mL×3), the organic phases were combined, washed with brine (50 mL), the organic phase was dried over anhydrous Na 2 SO 4 and concentrated. The crude product was stirred in 6N HCl (10 mL) at room temperature for 2 h, and then concentrated. The crude product was purified by column chromatography (EA/PE=30/70) to obtain the target product 1-(1,1-dioxo-2,3-di). Hydrobenzo[b]thiophen-4-yl)ethanone.
LC-MS:(ESI,m/z):[M+H] +＝210.1. LC-MS: (ESI, m/z): [M+H] + = 210.1.
步骤4：(E)-N-(1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 4: (E)-N-(1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethylene)-2-methylpropane-2 - Preparation of sulfenamides
Figure PCTCN2022088560-appb-000684
Figure PCTCN2022088560-appb-000684
将1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙酮(2.0g,9.5mmol)，Ti(OEt) 4(5.4g,1.6mmol)和(R)-丙烷-2-亚磺酰胺(1.7g,14.2mmol)在THF(40.0mL)中的反应液于70℃下搅拌反应4.0h。反应用冰水(100mL)淬灭，EA(80mL×3)萃取，合并有机相，用食盐水(30mL)洗，有机相经无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝50/50)纯化得目标产物(E)-N-(1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺。 1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethanone (2.0 g, 9.5 mmol), Ti(OEt) 4 (5.4 g, 1.6 mmol) ) and (R)-propane-2-sulfinamide (1.7 g, 14.2 mmol) in THF (40.0 mL) were stirred at 70 °C for 4.0 h. The reaction was quenched with ice water (100 mL), extracted with EA (80 mL×3), the organic phases were combined, washed with brine (30 mL), the organic phase was dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=50/50) to obtain the target product (E)-N-(1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophene-4). -yl)ethylene)-2-methylpropane-2-sulfenamide.
LC-MS:(ESI,m/z):[M+H] +＝314.2. LC-MS: (ESI, m/z): [M+H] + = 314.2.
步骤5：N-((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 5: N-((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)-2-methylpropane-2- Preparation of sulfenamides
Figure PCTCN2022088560-appb-000685
Figure PCTCN2022088560-appb-000685
0℃时向(E)-N-(1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)亚乙基)-2-甲基丙烷-2-亚磺酰胺(2.0g,6.3mmol)的THF/H 2O(20.0mL/4.0mL)的溶液中加入NaBH 4(0.5g,12.6mmol)。反应液于0℃下搅拌反应5.0min。反应用冰水(100mL)淬灭，EA(80mL×3)萃取，合并有机相，用食盐水(40mL)洗，有机相经无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝50/50)纯化得目标产物N-((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)-2-甲基丙烷-2-亚磺酰胺。 To (E)-N-(1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethylene)-2-methylpropane- To a solution of 2-sulfinamide (2.0 g, 6.3 mmol) in THF/ H2O (20.0 mL/ 4.0 mL) was added NaBH4 (0.5 g, 12.6 mmol). The reaction solution was stirred at 0 °C for 5.0 min. The reaction was quenched with ice water (100 mL), extracted with EA (80 mL×3), the organic phases were combined, washed with brine (40 mL), the organic phase was dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=50/50) to obtain the target product N-((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophene-4). -yl)ethyl)-2-methylpropane-2-sulfinamide.
LC-MS:(ESI,m/z):[M+H] +＝316.3. LC-MS: (ESI, m/z): [M+H] + = 316.3.
1H NMR(400MHz,CDCl 3)δ7.71(d,J＝7.7Hz,1H),7.67(d,J＝7.6Hz,1H),7.53(t,J＝7.6Hz,1H),4.76–4.66(m,1H),3.59–3.47(m,3H),3.43–3.28(m,2H),1.54(d,J＝6.6Hz,3H),1.24(s,9H). 1 H NMR (400 MHz, CDCl 3 ) δ 7.71 (d, J=7.7 Hz, 1H), 7.67 (d, J=7.6 Hz, 1H), 7.53 (t, J=7.6 Hz, 1H), 4.76-4.66 (m, 1H), 3.59–3.47 (m, 3H), 3.43–3.28 (m, 2H), 1.54 (d, J=6.6Hz, 3H), 1.24 (s, 9H).
步骤6：(R)-4-(1-氨乙基)-2,3-二氢苯并[b]噻吩1,1-二氧代盐酸盐的制备Step 6: Preparation of (R)-4-(1-aminoethyl)-2,3-dihydrobenzo[b]thiophene 1,1-dioxohydrochloride
Figure PCTCN2022088560-appb-000686
Figure PCTCN2022088560-appb-000686
将N-((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)-2-甲基丙烷-2-亚磺酰胺的盐酸二氧六环(4N,20.0mL)的溶液于25℃下搅拌反应2.0h。反应液浓缩。残余物用PE(20mL×2)洗，固体干燥得目标产物(R)-4-(1-氨乙基)-2,3-二氢苯并[b]噻吩1,1-二氧代盐酸盐。所得粗品直接用于下一步反应。N-((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)-2-methylpropane-2-sulfinyl A solution of the amide in dioxane hydrochloride (4N, 20.0 mL) was stirred at 25 °C for 2.0 h. The reaction solution was concentrated. The residue was washed with PE (20 mL×2), and the solid was dried to obtain the target product (R)-4-(1-aminoethyl)-2,3-dihydrobenzo[b]thiophene 1,1-dioxo salt acid salt. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝211.2. LC-MS: (ESI, m/z): [M+H] + = 211.2.
1HNMR(400MHz,DMSO-d 6)δ8.56(s,2H),7.94(d,J＝7.6Hz,1H),7.77(d,J＝7.5Hz,1H),7.67(d,J＝7.7Hz,1H),4.65–4.49(m,1H),3.69–3.56(m,2H),3.55-3.42(m,2H),1.54(d,J＝6.8Hz,3H). 1 HNMR (400MHz, DMSO-d 6 )δ8.56(s, 2H), 7.94(d, J=7.6Hz, 1H), 7.77(d, J=7.5Hz, 1H), 7.67(d, J=7.7 Hz, 1H), 4.65–4.49 (m, 1H), 3.69–3.56 (m, 2H), 3.55–3.42 (m, 2H), 1.54 (d, J=6.8Hz, 3H).
步骤7：(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 7: (1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl ) Amino)-7-methoxy-2-methylquinazolin-6-yl) cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000687
Figure PCTCN2022088560-appb-000687
将(R)-4-(1-氨乙基)-2,3-二氢苯并[b]噻吩1,1-二氧代(0.7g,3.3mmol)，DIEA(928.8mg,7.2mmol)和(1R,4R)-4-(4-氯-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(835.2mg,2.4mmol)在二氧六环(10.0mL)中的反应液于110℃下搅拌反应20.0h。反应用水(50mL)淬灭，EA(30.0mL×3)萃取，合并有机相，用食盐水(30mL)洗，无水Na 2SO 4干燥，浓缩。粗品经制备HPLC(乙腈/0.05％HCOOH水溶液,5％至95％)纯化得目标产物(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 (R)-4-(1-aminoethyl)-2,3-dihydrobenzo[b]thiophene 1,1-dioxo (0.7 g, 3.3 mmol), DIEA (928.8 mg, 7.2 mmol) and (1R,4R)-4-(4-chloro-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid methyl ester (835.2 mg, 2.4 mmol) in The reaction solution in dioxane (10.0 mL) was stirred at 110° C. for 20.0 h. The reaction was quenched with water (50 mL), extracted with EA (30.0 mL×3), the organic phases were combined, washed with brine (30 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous HCOOH, 5% to 95%) to give the desired product (1R,4R)-4-(4-(((R)-1-(1,1-dioxo- 2,3-Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝524.5. LC-MS: (ESI, m/z): [M+H] + = 524.5.
步骤8：(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 8: (1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl ) Amino)-7-methoxy-2-methylquinazolin-6-yl) preparation of cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000688
Figure PCTCN2022088560-appb-000688
向(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(100.0mg,0.2mmol)的THF/H 2O(2.0mL/1.0mL)溶液中加入LiOH(24mg,1.0mmol)。反应液于50℃下搅拌反应12.0h。反应液用1N HCl将pH调节至4-5，然后浓缩得目标产物(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。所得粗品直接用于下一步反应。 To (1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid methyl ester (100.0 mg, 0.2 mmol) in THF/H 2 O (2.0 mL/1.0 mL) To the solution was added LiOH (24 mg, 1.0 mmol). The reaction solution was stirred at 50 °C for 12.0 h. The pH of the reaction solution was adjusted to 4-5 with 1N HCl, and then concentrated to obtain the target product (1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3- Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝510.1. LC-MS: (ESI, m/z): [M+H] + = 510.1.
步骤9：4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯的制备Step 9: 4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl ) ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000689
Figure PCTCN2022088560-appb-000689
向(1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(110.0mg,0.2mmol)，哌嗪-1-羧酸叔丁酯(45.0mg,0.22mmol)和DIEA(85.0mg,0.6mmol)的DMF(2.0mL)溶液中加入HATU(124.0mg,0.24mmol)。反应液于室温下搅拌反应2.0h。反应用冰水(40mL)淬灭，然后将析出物过滤，滤饼真空干燥得目标产物4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯。所得粗品直接用于下一步反应。To (1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (110.0 mg, 0.2 mmol), tert-butyl piperazine-1-carboxylate (45.0 mg, 0.22 mmol) and DIEA (85.0 mg, 0.6 mmol) in DMF (2.0 mL) was added HATU (124.0 mg, 0.24 mmol). The reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched with ice water (40 mL), then the precipitate was filtered, and the filter cake was vacuum dried to obtain the target product 4-((1R,4R)-4-(4-((((R)-1-(1,1-) Dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperazine-1-carboxylate tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝678.1. LC-MS: (ESI, m/z): [M+H] + = 678.1.
步骤10：((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮的制备Step 10: ((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethane Preparation of (methyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000690
Figure PCTCN2022088560-appb-000690
将4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯(110.0mg,0.1mmol)的TFA/DCM(1.0mL/3.0mL)反应液于室温下搅拌反应1h。反应液浓缩得目标产物((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮。所得粗品直接用于下一步反应。4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethane (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester (110.0 mg, 0.1 mmol) in TFA /DCM (1.0 mL/3.0 mL) reaction solution was stirred at room temperature for 1 h. The reaction solution was concentrated to obtain the target product ((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophene-4- (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝578.2. LC-MS: (ESI, m/z): [M+H] + = 578.2.
步骤11：9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 11: 9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophene -4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3- Preparation of azaspiro[5.5]undecane-3-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000691
Figure PCTCN2022088560-appb-000691
向((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(60.0mg,0.1mmol)和9-甲醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(35.0mg,0.12mmol)的THF(5.0mL)溶液中加入STAB(64.0mg,0.3mmol)。反应液于室温下搅拌反应2.0h。反应用冰水(10mL)淬灭，EA(30.0mL X3)萃取，合并的有机相用食盐水(10mL)洗，无水Na 2SO 4干燥，浓缩。粗品经柱层析(MeOH/DCM,0-10％)纯化得目标产物9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To ((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone (60.0 mg, 0.1 mmol) and 9-carbaldehyde-3-aza To a solution of spiro[5.5]undecane-3-carboxylate tert-butyl ester (35.0 mg, 0.12 mmol) in THF (5.0 mL) was added STAB (64.0 mg, 0.3 mmol). The reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched with ice water (10 mL), extracted with EA (30.0 mL×3), the combined organic phases were washed with brine (10 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (MeOH/DCM, 0-10%) to obtain the target product 9-((4-((1R,4R)-4-(4-((((R)-1-(1,1-) Dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝843.3. LC-MS: (ESI, m/z): [M+H] + = 843.3.
步骤12：(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮的制备Step 12: (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R )-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- Preparation of 6-yl)cyclohexyl)methanone
Figure PCTCN2022088560-appb-000692
Figure PCTCN2022088560-appb-000692
将9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(70.0mg,0.08mmol)的TFA/DCM(1.0mL/3.0mL)反应液于室温下搅拌反应1.0h。反应液浓缩得目标产物(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮。所得粗品直接用于下一步反应。9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophene-4 -yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-aza The reaction solution of spiro[5.5]undecane-3-carboxylate tert-butyl ester (70.0 mg, 0.08 mmol) in TFA/DCM (1.0 mL/3.0 mL) was stirred at room temperature for 1.0 h. The reaction solution was concentrated to obtain the target product (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-( ((R)-1-(1,1-Dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexyl)methanone. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝743.3. LC-MS: (ESI, m/z): [M+H] + = 743.3.
步骤13：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 13: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-dioxo-2, 3-Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- Preparation of 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000693
Figure PCTCN2022088560-appb-000693
向(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(60.0mg,0.08mmol)的DMSO(1.0mL)溶液中加入DIEA(31.20mg,0.24mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(43.4mg,0.1mmol)。反应液于室温下搅拌反应2.0h。反应用水淬灭，EA萃取，合并的有机相用食盐水洗，无水干燥，浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得目标产物1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(1,1-二氧代-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)- 1-(1,1-Dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6- dimethyl)cyclohexyl)methanone (60.0 mg, 0.08 mmol) in DMSO (1.0 mL) was added DIEA (31.20 mg, 0.24 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)pentafluorophenyl benzoate (43.4 mg, 0.1 mmol). The reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched with water, extracted with EA, the combined organic phases were washed with brine, dried over anhydrous and concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(2-chloro-5-(9-((4-((1R,4R)-4- (4-(((R)-1-(1,1-dioxo-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)di Hydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝993.4. LC-MS: (ESI, m/z): [M+H] + = 993.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.29(d,J＝7.0Hz,1H),8.06(s,1H),7.80(d,J＝7.5Hz,1H),7.70-7.50(m,4H),7.39(dd,J＝8.2,1.9Hz,1H),6.98(s,1H),5.65-5.55(m,1H),3.87(s,3H),3.81-3.70(m,2H),3.68-3.52(m,4H),3.54-3.42(m,5H),2.98-2.91(m,1H),2.7-2.71(m,2H),2.70-2.62(m,1H),2.39-2.22(m,7H),2.18-2.10(m,2H),1.91-1.77(m,4H),1.75-1.18(m,19H),1.13-1.00(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.29 (d, J=7.0Hz, 1H), 8.06 (s, 1H), 7.80 (d, J=7.5Hz, 1H) ,7.70-7.50(m,4H),7.39(dd,J=8.2,1.9Hz,1H),6.98(s,1H),5.65-5.55(m,1H),3.87(s,3H),3.81-3.70 (m,2H),3.68-3.52(m,4H),3.54-3.42(m,5H),2.98-2.91(m,1H),2.7-2.71(m,2H),2.70-2.62(m,1H) ,2.39-2.22(m,7H),2.18-2.10(m,2H),1.91-1.77(m,4H),1.75-1.18(m,19H),1.13-1.00(m,4H).
实施例11：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 11: 1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propyl)piperidine-1 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙基)哌嗪-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000694
Figure PCTCN2022088560-appb-000694
将4-(3-(甲苯磺酰氧基)丙基)哌啶-1-羧酸叔丁酯(500mg,2.3mmol)，哌嗪-1-羧酸苄酯(1.0g,2.7mmol),K 2CO 3(1.5g,11.3mmol)和KI(450.0mg,2.7mmol)在DMF(10.0mL)中的反应液于70℃下搅拌反应过夜。反应用冰水(100mL)淬灭，EA(30mL×3)萃取，合并的有机相经食盐水(15mL)洗，无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝0-30％)纯化得目标产物4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙基)哌嗪-1-羧酸苄酯。 4-(3-(Tosyloxy)propyl)piperidine-1-carboxylate tert-butyl ester (500mg, 2.3mmol), piperazine-1-carboxylate benzyl ester (1.0g, 2.7mmol), A reaction of K 2 CO 3 (1.5 g, 11.3 mmol) and KI (450.0 mg, 2.7 mmol) in DMF (10.0 mL) was stirred at 70° C. overnight. The reaction was quenched with ice water (100 mL), extracted with EA (30 mL×3), the combined organic phases were washed with brine (15 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=0-30%) to obtain the target product 4-(3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)piperazine-1-carboxylic acid benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝446.5. LC-MS: (ESI, m/z): [M+H] + = 446.5.
步骤2：4-(3-(哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(3-(piperazin-1-yl)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000695
Figure PCTCN2022088560-appb-000695
将4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙基)哌嗪-1-羧酸苄酯(400.0mg,0.6mmol)和Pd(OH) 2/C(10％,100.0mg)在EtOAc(20.0mL)中的反应液于70℃下H 2(60psi)下搅拌反应12.0h。反应液经硅藻土过滤，滤饼用EA(10mL×2)冲洗，合并滤液并浓缩得目标产物4-(3-(哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯。所得粗品直接用于下一步反应。 Benzyl 4-(3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)piperazine-1-carboxylate (400.0 mg, 0.6 mmol) and Pd(OH) 2 /C ( 10%, 100.0 mg) in EtOAc (20.0 mL) The reaction was stirred at 70 °C under H2 (60 psi) for 12.0 h. The reaction solution was filtered through celite, the filter cake was washed with EA (10 mL×2), the filtrates were combined and concentrated to obtain the target product 4-(3-(piperazin-1-yl)propyl)piperidine-1-carboxylic acid tertiary Butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝312.2. LC-MS: (ESI, m/z): [M+H] + = 312.2.
步骤3：4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯的制备Step 3: 4-(3-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5- (Trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propyl)piperidine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000696
Figure PCTCN2022088560-appb-000696
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基-1-羧酸(85.0mg,0.2mmol)，4-(3-(哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯(68.0mg,0.22mmol)和DIEA(59.0mg, 0.6mmol)的DMF(2.0mL)溶液中加入HATU(91.0mg,0.24mmol)。反应液于室温下搅拌反应2.0h。反应用冰水(20mL)淬灭，过滤收集析出物，用水(10mL×2)冲洗，干燥得目标产物4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexyl-1-carboxylic acid (85.0 mg, 0.2 mmol), tert-4-(3-(piperazin-1-yl)propyl)piperidine-1-carboxylic acid To a solution of butyl ester (68.0 mg, 0.22 mmol) and DIEA (59.0 mg, 0.6 mmol) in DMF (2.0 mL) was added HATU (91.0 mg, 0.24 mmol). The reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched with ice water (20 mL), the precipitate was collected by filtration, rinsed with water (10 mL×2), and dried to obtain the target product 4-(3-(4-((1R,4R)-4-(7-methoxyl) -2-Methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane- 1-Carbonyl)piperazin-1-yl)propyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝826.5. LC-MS: (ESI, m/z): [M+H] + = 826.5.
步骤4：4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯的制备Step 4: 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propyl)piperidine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000697
Figure PCTCN2022088560-appb-000697
将4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯(130.0mg,0.18mmol)和10％Pd/C(30.0mg)的MeOH(10.0mL)反应液于60℃下H 2(90psi)下搅拌反应过夜。反应液经硅藻土过滤，滤液浓缩得目标产物4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯。所得粗品直接用于下一步反应。 4-(3-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tri Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexyl-1-carbonyl)piperazin-1-yl)propyl)piperidine-1-carboxylate tert-butyl ester (130.0 mg , 0.18 mmol) and 10% Pd/C (30.0 mg) in MeOH (10.0 mL) The reaction was stirred overnight at 60 °C under H 2 (90 psi). The reaction solution was filtered through celite, and the filtrate was concentrated to obtain the target product 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(tri Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propyl)piperidine tert-butyl pyridine-1-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝796.5. LC-MS: (ESI, m/z): [M+H] + =796.5.
步骤5：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌嗪-1-基)甲酮的制备Step 5: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000698
Figure PCTCN2022088560-appb-000698
将4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基-1-羰基)哌嗪-1-基)丙基)哌啶-1-羧酸叔丁酯(100.0mg,0.1mmol)的TFA/DCM(1.0mL/3.0mL)反应液于室温下搅拌反应1h。反应液浓缩得目标产物((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌嗪-1-基)甲酮。4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexyl-1-carbonyl)piperazin-1-yl)propyl)piperidine-1-carboxylate tert-butyl ester (100.0 mg, 0.1 mmol) TFA/DCM (1.0 mL/3.0 mL) reaction solution was stirred at room temperature for 1 h. The reaction solution was concentrated to obtain the target product ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperazin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝696.3. LC-MS: (ESI, m/z): [M+H] + = 696.3.
步骤6：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propyl)piperidine-1- Preparation of carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000699
Figure PCTCN2022088560-appb-000699
向((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌嗪-1-基)甲酮(100mg,0.14mmol)的DMSO(5.0mL)溶液中加入DIEA(103mg,0.8mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(73mg,0.17mmol)，反应液于室温下搅拌反应2.0h。反应用水(15mL)淬灭，EA(30.0mL×3)萃取，合并有机相，并用食盐水(15mL)洗，无水Na 2SO 4干燥，反应液浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得目标产物1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperazin-1-yl)methanone (100 mg, 0.14 mmol) in DMSO (5.0 mL) solution was added DIEA (103 mg, 0.8 mmol) and pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (73 mg, 0.17 mmol) ), the reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched with water (15 mL), extracted with EA (30.0 mL×3), the organic phases were combined, washed with brine (15 mL), dried over anhydrous Na 2 SO 4 , and the reaction solution was concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(5-(4-(3-(4-((1R,4R)-4-(4 -(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cycle Hexane-1-carbonyl)piperazin-1-yl)propyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝946.4. LC-MS: (ESI, m/z): [M+H] + = 946.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.13(d,J＝5.5Hz,1H),8.06(s,1H),7.63(d,J＝8.2Hz, 1H),7.54(d,J＝1.6Hz,1H),7.38(d,J＝8.4Hz,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.63–5.50(m,3H),4.44(s,1H),3.89(s,3H),3.79-3.74(m,1H),3.64–3.59(m,1H),3.48-3.41(m,4H),3.18-2.90(m,2H),2.78–2.62(m,4H),2.38-2.21(m,9H),1.90–1.43(m,17H),1.24-1.19(m,2H),1.10-1.08(m,2H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.13 (d, J=5.5 Hz, 1H), 8.06 (s, 1H), 7.63 (d, J=8.2 Hz, 1H) ,7.54(d,J＝1.6Hz,1H),7.38(d,J＝8.4Hz,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.70(s, 1H), 5.63–5.50(m, 3H), 4.44(s, 1H), 3.89(s, 3H), 3.79-3.74(m, 1H), 3.64–3.59(m, 1H), 3.48-3.41(m, 4H), 3.18-2.90(m, 2H), 2.78-2.62(m, 4H), 2.38-2.21(m, 9H), 1.90-1.43(m, 17H), 1.24-1.19(m, 2H), 1.10- 1.08(m,2H).
实施例12：1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 12: 1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-(1-(叔丁氧羰基)哌啶-4-基)乙基)哌嗪-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000700
Figure PCTCN2022088560-appb-000700
将4-(2-(甲苯磺酰氧基)乙基)哌啶-1-羧酸叔丁酯(500.0mg,2.3mmol),哌嗪-1-羧酸苄酯(1.0g,2.7mmol)，K 2CO 3(1.5g,11.3mmol)和KI(450.0mg,2.7mmol)在DMF(10.0mL)中的反应液于70℃下搅拌反应过夜。反应用冰水(100mL)淬灭，EA(30.0mL×3)萃取，合并的有机相经食盐水(20mL)洗，无水Na 2SO 4干燥，浓缩。粗品经柱层析(EA/PE＝0-30％)纯化得目标产物4-(2-(1-(叔丁氧羰基)哌啶-4-基)乙基)哌嗪-1-羧酸苄酯。 4-(2-(Tosyloxy)ethyl)piperidine-1-carboxylic acid tert-butyl ester (500.0 mg, 2.3 mmol), piperazine-1-carboxylic acid benzyl ester (1.0 g, 2.7 mmol) , K 2 CO 3 (1.5 g, 11.3 mmol) and KI (450.0 mg, 2.7 mmol) in DMF (10.0 mL) were stirred overnight at 70 °C. The reaction was quenched with ice water (100 mL), extracted with EA (30.0 mL×3), the combined organic phases were washed with brine (20 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by column chromatography (EA/PE=0-30%) to obtain the target product 4-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)piperazine-1-carboxylic acid benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝432.7. LC-MS: (ESI, m/z): [M+H] + = 432.7.
步骤2：4-(2-(哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(2-(piperazin-1-yl)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000701
Figure PCTCN2022088560-appb-000701
将4-(2-(1-(叔丁氧羰基)哌啶-4-基)乙基)哌嗪-1-羧酸苄酯(400.0mg,0.6mmol)和10％Pd(OH) 2/C(100mg)在EtOAc(20mL)中的反应液于70℃下H 2(60psi)下搅拌反应12h。反应液经硅藻土过滤，滤饼用EA(10mL×2)冲洗，滤液浓缩得目标产物4-(2-(哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯。 Benzyl 4-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)piperazine-1-carboxylate (400.0 mg, 0.6 mmol) and 10% Pd(OH) 2 / The reaction of C (100 mg) in EtOAc (20 mL) was stirred at 70 °C under H2 (60 psi) for 12 h. The reaction solution was filtered through celite, the filter cake was rinsed with EA (10 mL×2), and the filtrate was concentrated to obtain the target product, tert-butyl 4-(2-(piperazin-1-yl)ethyl)piperidine-1-carboxylate .
LC-MS:(ESI,m/z):[M+H] +＝298.2. LC-MS: (ESI, m/z): [M+H] + = 298.2.
步骤3：4-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯的制备Step 3: 4-(2-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5- (Trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000702
Figure PCTCN2022088560-appb-000702
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸(85.0mg,0.2mmol)，4-(2-(哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯(68.0mg,0.22mmol)和DIEA(59.0mg,0.6mmol)的DMF(2.0mL)溶液中加入HATU(91.0mg,0.24mmol)。反应液于室温下搅拌反应2h。反应用冰水(20.0mL)淬灭，过滤收集析出物，并用水(10mL×2)冲洗，真空干燥得目标产物4-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid (85.0 mg, 0.2 mmol), 4-(2-(piperazin-1-yl)ethyl)piperidine-1-carboxylic acid To a solution of tert-butyl ester (68.0 mg, 0.22 mmol) and DIEA (59.0 mg, 0.6 mmol) in DMF (2.0 mL) was added HATU (91.0 mg, 0.24 mmol). The reaction solution was stirred at room temperature for 2 h. The reaction was quenched with ice water (20.0 mL), the precipitate was collected by filtration, rinsed with water (10 mL×2), and dried in vacuo to obtain the target product 4-(2-(4-((1R,4R)-4-(7- Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cycle Hexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝812.5. LC-MS: (ESI, m/z): [M+H] + = 812.5.
步骤4：4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯的制备Step 4: 4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000703
Figure PCTCN2022088560-appb-000703
将4-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯(130mg,0.18mmol)和10％Pd/C(30mg)在MeOH(10mL)中的反应液在60℃下H 2(90psi)下搅拌反应过夜。反应液经硅藻土过滤，滤饼用甲醇(5mL×2)冲洗，合并滤液并浓缩得目标产物4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯。 4-(2-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tri Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester (130 mg , 0.18 mmol) and 10% Pd/C (30 mg) in MeOH (10 mL) was stirred overnight at 60 °C under H2 (90 psi). The reaction solution was filtered through celite, the filter cake was washed with methanol (5 mL×2), the filtrates were combined and concentrated to obtain the target product 4-(2-(4-((1R,4R)-4-(4-((((R )-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝782.5. LC-MS: (ESI, m/z): [M+H] + = 782.5.
步骤5：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌嗪-1-基)甲酮的制备Step 5: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-yl)ethyl)piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000704
Figure PCTCN2022088560-appb-000704
将4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羧酸叔丁酯(100mg,0.1mmol)在TFA/DCM(1mL/3mL)中的反应液在室温下搅拌反应1.0h。反应液浓缩得目标产物((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌嗪-1-基)甲酮。4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carboxylate tert-butyl ester (100mg, 0.1 mmol) in TFA/DCM (1 mL/3 mL) was stirred at room temperature for 1.0 h. The reaction solution was concentrated to obtain the target product ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-yl)ethyl)piperazin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝682.2. LC-MS: (ESI, m/z): [M+H] + = 682.2.
步骤6：1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1- Preparation of carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000705
Figure PCTCN2022088560-appb-000705
向((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌嗪-1-基)甲酮(100mg,0.14mmol)的DMSO(5.0mL)溶液中加入DIEA(103mg,0.8mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(73mg,0.17mmol)，反应液于室温下搅拌反应2.0h。反应液用水(15mL)淬灭，EA(30mL×3)萃取，合并的有机相用食盐水(20mL)洗，无水Na 2SO 4干燥，浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液，5％至95％)纯化得目标产物1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-yl)ethyl)piperazin-1-yl)methanone (100 mg, 0.14 mmol) in DMSO (5.0 mL) solution was added DIEA (103 mg, 0.8 mmol) and pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (73 mg, 0.17 mmol) ), the reaction solution was stirred at room temperature for 2.0 h. The reaction solution was quenched with water (15 mL), extracted with EA (30 mL×3), the combined organic phases were washed with brine (20 mL), dried over anhydrous Na 2 SO 4 and concentrated. The crude product was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(5-(4-(2-(4-((1R,4R)-4-(4 -(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cycle Hexane-1-carbonyl)piperazin-1-yl)ethyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝932.4. LC-MS: (ESI, m/z): [M+H] + = 932.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.12(d,J＝7.6Hz,1H),8.06(s,1H),7.64(d,J＝8.2Hz,1H),7.54(s,1H),7.38(d,J＝8.3Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65-5.50(m,3H),4.50-4.40(m,1H),3.88(s,3H),3.78-3.72(m,1H),3.68-3.61(m,1H),3.52-3.41(m,4H),3.07-2.91(m,2H),2.77-2.60(m,3H),2.38-2.30(m,9H),1.88-1.52(m,16H),1.45-1.35(m,2H),1.28-1.01(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.12(d, J=7.6Hz, 1H), 8.06(s, 1H), 7.64(d, J=8.2Hz, 1H) ,7.54(s,1H),7.38(d,J=8.3Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65- 5.50(m,3H),4.50-4.40(m,1H),3.88(s,3H),3.78-3.72(m,1H),3.68-3.61(m,1H),3.52-3.41(m,4H), 3.07-2.91(m, 2H), 2.77-2.60(m, 3H), 2.38-2.30(m, 9H), 1.88-1.52(m, 16H), 1.45-1.35(m, 2H), 1.28-1.01(m , 2H).
实施例13：1-(5-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 13: 1-(5-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carbonyl )-2-Chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-((1-(叔丁氧羰基)哌啶-4-基)甲基)哌嗪-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-((1-(tert-butoxycarbonyl)piperidin-4-yl)methyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000706
Figure PCTCN2022088560-appb-000706
向哌嗪-1-羧酸苄酯(500.0mg,2.27mmol)和4-甲醛哌啶-1-羧酸叔丁酯(726.5.0mg,3.4mmol)的THF(10.0mL)中缓慢加入STAB(1.2g,5.5mmol)，反应液于室温下搅拌反应过夜。反应用水(20mL)淬灭，EA (20mL×2)萃取，有机相经无水Na 2SO 4干燥，浓缩得到粗产物。粗品经柱层析(EA/PE＝10/90)纯化得目标产物4-((1-(叔丁氧羰基)哌啶-4-基)甲基)哌嗪-1-羧酸苄酯。 To benzyl piperazine-1-carboxylate (500.0 mg, 2.27 mmol) and tert-butyl 4-carbaldehyde piperidine-1-carboxylate (726.5.0 mg, 3.4 mmol) in THF (10.0 mL) was slowly added STAB ( 1.2 g, 5.5 mmol), the reaction solution was stirred at room temperature overnight. The reaction was quenched with water (20 mL), extracted with EA (20 mL×2), and the organic phase was dried over anhydrous Na 2 SO 4 and concentrated to obtain the crude product. The crude product was purified by column chromatography (EA/PE=10/90) to obtain the target product, benzyl 4-((1-(tert-butoxycarbonyl)piperidin-4-yl)methyl)piperazine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝418.1. LC-MS: (ESI, m/z): [M+H] + = 418.1.
步骤2：4-(哌嗪-1-基甲基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(piperazin-1-ylmethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000707
Figure PCTCN2022088560-appb-000707
向4-((1-(叔-丁氧基羰基)哌啶-4-基)甲基)哌嗪-1-羧酸苄酯的EtOAc(15.0mL)中加入Pd(OH) 2/C(300.0mg,0.36mmol)，反应液于80℃下H 2氛围下搅拌反应过夜。反应液过滤，浓缩得到目标产物4-(哌嗪-1-基甲基)哌啶-1-羧酸叔丁酯。所得粗品直接用于下一步反应。 To benzyl 4-((1-(tert-butoxycarbonyl)piperidin-4-yl)methyl)piperazine-1-carboxylate in EtOAc (15.0 mL) was added Pd(OH) 2 /C( 300.0 mg, 0.36 mmol), the reaction solution was stirred at 80 °C under H 2 atmosphere overnight. The reaction solution was filtered and concentrated to obtain the target product 4-(piperazin-1-ylmethyl)piperidine-1-carboxylate tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝284.1. LC-MS: (ESI, m/z): [M+H] + = 284.1.
步骤3：(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸的制备Step 3: (1R,4R)-4-(7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl) Preparation of ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000708
Figure PCTCN2022088560-appb-000708
向(1R,4r)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯(100.0mg,0.2mmol)的THF/H 2O(1:1)溶液中加入LiOH(9.60mg,0.4mmol)，反应液于室温下搅拌反应16h。反应液用1N HCl将pH调节至4-5，然后用MeOH/CH 2Cl 2(1/10，10.0mL×2)混合溶剂萃取。有机相经Na 2SO 4干燥，浓缩得到目标产物(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸。所得粗品直接用于下一步反应。 To (1R,4r)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (100.0 mg, 0.2 mmol) in THF/H 2 O (1:1) was added LiOH (9.60 mg, 0.4 mmol) , the reaction solution was stirred at room temperature for 16h. The pH of the reaction solution was adjusted to 4-5 with 1N HCl, and then extracted with a mixed solvent of MeOH/CH 2 Cl 2 (1/10, 10.0 mL×2). The organic phase was dried over Na 2 SO 4 and concentrated to give the target product (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5 -(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝533.1. LC-MS: (ESI, m/z): [M+H] + = 533.1.
步骤4：4-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯的制备Step 4: 4-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tris) Preparation of fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000709
Figure PCTCN2022088560-appb-000709
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸(90.00mg,0.17mmol)的DMF(5.0mL)溶液中加入DIEA(65.20mg,0.52mmol)，HATU(197.6mg,0.52mmol)和4-(哌嗪-1-基甲基)哌啶-1-羧酸叔丁酯(57.6mg,0.2mmol)。反应液在室温下搅拌反应5h。反应液用水(40mL)稀释，EA(20mL×3)萃取。有机相经Na 2SO 4干燥，浓缩。所得粗品经柱层析(EA/PE＝50/50)纯化得到目标产物4-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯。 To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid (90.00 mg, 0.17 mmol) in DMF (5.0 mL) was added DIEA (65.20 mg, 0.52 mmol), HATU (197.6 mg, 0.52 mmol) mmol) and tert-butyl 4-(piperazin-1-ylmethyl)piperidine-1-carboxylate (57.6 mg, 0.2 mmol). The reaction solution was stirred at room temperature for 5h. The reaction solution was diluted with water (40 mL) and extracted with EA (20 mL×3). The organic phase was dried over Na2SO4 and concentrated. The obtained crude product was purified by column chromatography (EA/PE=50/50) to obtain the target product 4-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(( (R)-1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl ) methyl) piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝798.2. LC-MS: (ESI, m/z): [M+H] + = 798.2.
步骤5：4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯的制备Step 5: 4-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) Preparation of -7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carboxylic acid tert-butyl ester
Figure PCTCN2022088560-appb-000710
Figure PCTCN2022088560-appb-000710
向4-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己 烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯(40mg,0.05mmol)的EA(15.0mL)溶液中加入Pd/C(15.0mg)。反应液在80℃下H 2氛围下搅拌反应16h。反应液过滤，并用EA(10mL×2)冲洗滤饼。有机相浓缩得到目标产物4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯。所得粗品直接用于下一步。 to 4-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carboxylate tert-butyl ester (40 mg, 0.05 mmol) in EA (15.0 mL) was added Pd/C (15.0 mg). The reaction solution was stirred at 80 °C under H 2 atmosphere for 16 h. The reaction solution was filtered, and the filter cake was washed with EA (10 mL×2). The organic phase was concentrated to obtain the target product 4-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carboxylate tert-butyl ester . The resulting crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝768.3. LC-MS: (ESI, m/z): [M+H] + = 768.3.
步骤6：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(哌啶-4-基甲基)哌嗪-1-基)甲酮的制备Step 6: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-(piperidin-4-ylmethyl)piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000711
Figure PCTCN2022088560-appb-000711
将4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羧酸叔丁酯(30mg,0.04mmol)的TFA/DCM(3.0mL,1:5)溶液在室温下搅拌反应2h。反应液浓缩得到目标产物((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(哌啶-4-基甲基)哌嗪-1-基)甲酮。所得粗品直接用于下一步。4-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carboxylate tert-butyl ester (30 mg, 0.04 mmol ) in TFA/DCM (3.0 mL, 1:5) was stirred at room temperature for 2 h. The reaction solution was concentrated to obtain the target product ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(piperidin-4-ylmethyl)piperazin-1-yl)methanone. The resulting crude product was used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝668.3. LC-MS: (ESI, m/z): [M+H] + = 668.3.
步骤7：1-(5-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(5-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1-carbonyl) Preparation of -2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000712
Figure PCTCN2022088560-appb-000712
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(哌啶-4-基甲基)哌嗪-1-基)甲酮(25.0mg,0.037mmol)的DMSO(5.0mL)溶液中加入DIEA(14.50mg,0.112mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(19.30mg,0.044mmol)。反应液在室温下搅拌反应5h。反应液中加水(50mL)稀释，EtOAc(25mL×3)萃取，合并有机相，有机相用食盐水(10mL)洗，Na 2SO 4干燥，浓缩。粗品经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)得到目标产物1-(5-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 - Methylquinazolin-6-yl)cyclohexyl)(4-(piperidin-4-ylmethyl)piperazin-1-yl)methanone (25.0 mg, 0.037 mmol) in DMSO (5.0 mL) DIEA (14.50 mg, 0.112 mmol) and pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (19.30 mg, 0.044 mmol) were added to it . The reaction solution was stirred at room temperature for 5h. The reaction solution was diluted with water (50 mL), extracted with EtOAc (25 mL×3), the organic phases were combined, washed with brine (10 mL), dried over Na 2 SO 4 and concentrated. The crude product was subjected to preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(5-(4-((4-((1R,4R)-4-(4-(( (R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperazin-1-yl)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝918.4. LC-MS: (ESI, m/z): [M+H] + = 918.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.20-8.04(m,2H),7.64(s,1H),7.54(s,1H),7.38(s,1H),6.99(s,1H),6.93-6.83(m,2H),6.70(s,1H),5.60-5.45(m,3H),4.54-4.44(m,1H),3.98-3.80(m,4H),3.80-3.67(m,2H),3.05-2.90(m,2H),2.84-2.60(m,5H),2.45-2.10(m,10H),1.92-1.40(m,16H),1.15-0.98(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s,1H),8.20-8.04(m,2H),7.64(s,1H),7.54(s,1H),7.38(s,1H), 6.99(s,1H),6.93-6.83(m,2H),6.70(s,1H),5.60-5.45(m,3H),4.54-4.44(m,1H),3.98-3.80(m,4H), 3.80-3.67(m, 2H), 3.05-2.90(m, 2H), 2.84-2.60(m, 5H), 2.45-2.10(m, 10H), 1.92-1.40(m, 16H), 1.15-0.98(m , 2H).
实施例14：1-(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 14: 1-(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(哌啶-4-基)丙基)哌啶-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(3-(piperidin-4-yl)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000713
Figure PCTCN2022088560-appb-000713
将1,3-二(哌啶-4-基)丙烷(6.0g,28.6mmol)溶于乙腈/水(1:1,720mL)中，加入NaHCO 3(12.21g,71.5mmol)和CbzCl(4.88g,28.6mmol)，室温搅拌过夜，减压浓缩，用MeOH/DCM(1/10,200mL×5)提取，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(20％MeOH/DCM,0.1％氨水)纯化得到目标产物4-(3-(哌啶-4-基)丙基)哌啶-1-羧酸苄酯。 1,3-Bis(piperidin-4-yl)propane (6.0 g, 28.6 mmol) was dissolved in acetonitrile/water (1:1, 720 mL), NaHCO3 (12.21 g, 71.5 mmol) and CbzCl (4.88 g were added) , 28.6 mmol), stirred at room temperature overnight, concentrated under reduced pressure, extracted with MeOH/DCM (1/10, 200 mL×5), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (20% MeOH/DCM). , 0.1% ammonia water) to obtain the target product, benzyl 4-(3-(piperidin-4-yl)propyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝345.2. LC-MS: (ESI, m/z): [M+H] + = 345.2.
步骤2：4-(3-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基l)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯的制备Step 2: 4-(3-(1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5- (Trifluoromethyll)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester preparation
Figure PCTCN2022088560-appb-000714
Figure PCTCN2022088560-appb-000714
向(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸(120mg,0.225mmol)的DMF(10mL)溶液中，加入4-(3-(哌啶-4-基)丙基)哌啶-1-羧酸苄酯(116mg,0.337mmol)，HATU(110mg,0.292mmol)和DIEA(87mg,0.675mmol)，室温搅拌2小时，加水(100mL)并搅拌10min，用乙酸乙酯(100mL×3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(100％EA/PE)纯化得到目标产物4-(3-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基l)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯。To (1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl ) amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid (120 mg, 0.225 mmol) in DMF (10 mL) was added 4-(3-(piperidin-4-yl)propyl) Benzyl piperidine-1-carboxylate (116 mg, 0.337 mmol), HATU (110 mg, 0.292 mmol) and DIEA (87 mg, 0.675 mmol), stirred at room temperature for 2 hours, added water (100 mL) and stirred for 10 min, washed with ethyl acetate ( 100mL×3) extraction, the organic phase was washed with saturated brine (150mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (100% EA/PE) to obtain the target product 4-(3- (1-((1R,4R)-4-(7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)benzene yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝859.5. LC-MS: (ESI, m/z): [M+H] + = 859.5.
步骤3：4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯的制备Step 3: 4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl1)phenyl)ethyl) ) amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester preparation
Figure PCTCN2022088560-appb-000715
Figure PCTCN2022088560-appb-000715
向4-(3-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基l)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯(110mg,0.13mmol)的EtOH(10mL)溶液中，加入Raney-Ni(0.2mL)，N 2H 4-H 2O(0.2mL)，室温搅拌0.5h，过滤，减压浓缩得到产物4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯。 To 4-(3-(1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tri Fluoromethyl 1)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester (110mg , 0.13 mmol) in EtOH (10 mL) solution, added Raney-Ni (0.2 mL), N 2 H 4 -H 2 O (0.2 mL), stirred at room temperature for 0.5 h, filtered, and concentrated under reduced pressure to obtain the product 4-(3 -(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyll)phenyl)ethyl)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝829.4. LC-MS: (ESI, m/z): [M+H] + = 829.4.
步骤4：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌啶-1-基)甲酮的制备Step 4: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyll)phenyl)ethyl)amino)-7-methoxy Preparation of yl-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperidin-1-yl)methanone
Figure PCTCN2022088560-appb-000716
Figure PCTCN2022088560-appb-000716
向4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羧酸苄酯(85mg,0.1mmol)的乙酸乙酯溶液(10mL)中加入Pd(OH) 2/C(10mg)，在75℃下氢气氛围下搅拌8h，过滤，减压浓缩得到((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌啶-1-基)甲酮。 to 4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyll)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carboxylate benzyl ester (85mg, 0.1 mmol) in ethyl acetate solution (10 mL) was added Pd(OH) 2 /C (10 mg), stirred at 75° C. under a hydrogen atmosphere for 8 h, filtered, and concentrated under reduced pressure to obtain ((1R,4R)-4-( 4-(((R)-1-(3-amino-5-(trifluoromethyll)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl )cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperidin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝695.4. LC-MS: (ESI, m/z): [M+H] + = 695.4.
步骤5：1-(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1- Preparation of carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000717
Figure PCTCN2022088560-appb-000717
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基l)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙基)哌啶-1-基)甲酮(60mg,0.09mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(41mg,0.095mmol)用DMSO(5mL)溶解，DIEA(35mg,0.27mmol)加入，然后反应液室温搅拌2小时，水(50mL)加入到反应液中，搅拌2分钟，过滤，固体使用柱层析(10％MeOH/DCM)纯化后，再通过p-TLC纯化目标产物1-(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyll)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propyl)piperidin-1-yl)methanone (60 mg, 0.09 mmol) and 4- Pentafluorophenyl chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (41 mg, 0.095 mmol) was dissolved in DMSO (5 mL), DIEA (35 mg, 0.27 mmol) Add, then the reaction solution was stirred at room temperature for 2 hours, water (50 mL) was added to the reaction solution, stirred for 2 minutes, filtered, the solid was purified by column chromatography (10% MeOH/DCM), and then the target product 1 was purified by p-TLC -(5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carbonyl)-2 -Chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝945.2. LC-MS: (ESI, m/z): [M+H] + = 945.2.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.20-8.04(m,2H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.7Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65–5.44(m,3H),4.55-4.40(m,2H),3.98-3.84(m,4H),3.80-3.70(m,1H),3.66-3.48(m,2H),3.30-3.20(m,1H),3.10-2.90(m,3H),2.78-2.60(m,4H),2.48-2.40(m,2H),2.39-2.30(m,2H),1.90-1.42(m,14H),1.24-0.83(m,12H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 8.20-8.04(m, 2H), 7.63(d, J=8.2Hz, 1H), 7.54(d, J=1.7Hz, 1H), 7.38(dd, J=8.2, 1.8Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65–5.44(m ,3H),4.55-4.40(m,2H),3.98-3.84(m,4H),3.80-3.70(m,1H),3.66-3.48(m,2H),3.30-3.20(m,1H),3.10 -2.90(m, 3H), 2.78-2.60(m, 4H), 2.48-2.40(m, 2H), 2.39-2.30(m, 2H), 1.90-1.42(m, 14H), 1.24-0.83(m, 12H).
实施例15：1-(5-(4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 15: 1-(5-(4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：1,2-二(哌啶-4-基)乙烷的制备Step 1: Preparation of 1,2-bis(piperidin-4-yl)ethane
Figure PCTCN2022088560-appb-000718
Figure PCTCN2022088560-appb-000718
将Pd/C(1.2g,11.32mmol)加入到1,2-二(吡啶-4-基)乙烷(4.0g,21.74mmol)的IPA/H 2O溶液(120mL/140mL)中，在充满H 2的高压釜中，75℃搅拌72h，过滤，用二氯甲烷(100mL×4)润洗，减压浓缩得到目标产物1,2-二(哌啶-4-基)乙烷。 Pd/C (1.2 g, 11.32 mmol) was added to a solution of 1,2-bis(pyridin-4-yl)ethane (4.0 g, 21.74 mmol) in IPA/H 2 O (120 mL/140 mL), filled with In an autoclave of H2 , stirred at 75 °C for 72 h, filtered, rinsed with dichloromethane (100 mL × 4), and concentrated under reduced pressure to obtain the target product 1,2-bis(piperidin-4-yl)ethane.
LC-MS:(ESI,m/z):[M+H] +＝197.2. LC-MS: (ESI, m/z): [M+H] + = 197.2.
步骤2：4-(2-(哌啶-4-基)乙基)哌啶-1-羧酸苄酯的制备Step 2: Preparation of benzyl 4-(2-(piperidin-4-yl)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000719
Figure PCTCN2022088560-appb-000719
将NaHCO 3(1.0g,11.9mmol)和CbzCl(0.872g,5.10mmol)加入到1,2-二(哌啶-4-基)乙烷(1.0g,5.10mmol)的ACN/H 2O(60mL/60mL)中，常温搅拌过夜，加水(200mL)并搅拌10min，用乙酸乙酯(100mL×3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(30％ACN/H 2O)纯化得到目标产物4-(2-(哌啶-4-基)乙基)哌啶-1-羧酸苄酯。 NaHCO3 (1.0 g, 11.9 mmol) and CbzCl (0.872 g, 5.10 mmol) were added to 1,2-bis(piperidin-4-yl)ethane (1.0 g, 5.10 mmol) in ACN/ H2O ( 60mL/60mL), stirred overnight at room temperature, added water (200mL) and stirred for 10min, extracted with ethyl acetate (100mL×3), washed the organic phase with saturated brine (150mL), dried over anhydrous sodium sulfate, filtered, and reduced pressure. After concentration, the crude product was purified by column chromatography (30% ACN/ H2O ) to give the desired product benzyl 4-(2-(piperidin-4-yl)ethyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝331.4. LC-MS: (ESI, m/z): [M+H] + = 331.4.
步骤3：4-(2-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯的制备Step 3: 4-(2-(1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5- (trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate benzyl ester preparation
Figure PCTCN2022088560-appb-000720
Figure PCTCN2022088560-appb-000720
向4-(2-(哌啶-4-基)乙基)哌啶-1-羧酸苄酯(160mg,0.477mmol)的DMF(20mL)溶液中，加入(1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸(170mg,0.319mmol)，HATU(182.14mg，0.479mmol)和DIEA(123.66mg，0.9586mmol)，室温搅拌过夜，加水(200mL)并搅拌10min，用乙酸乙酯(100mL×3)提取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(20％EA/PE)纯化得到目标产物4-(2-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯。To a solution of benzyl 4-(2-(piperidin-4-yl)ethyl)piperidine-1-carboxylate (160 mg, 0.477 mmol) in DMF (20 mL) was added (1R,4R)-4-( 7-Methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl ) cyclohexane-1-carboxylic acid (170 mg, 0.319 mmol), HATU (182.14 mg, 0.479 mmol) and DIEA (123.66 mg, 0.9586 mmol), stirred at room temperature overnight, added water (200 mL) and stirred for 10 min, washed with ethyl acetate (100 mL×3) extraction, the organic phase was washed with saturated brine (150 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (20% EA/PE) to obtain the target product 4-(2 -(1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)benzene) yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝845.7. LC-MS: (ESI, m/z): [M+H] + = 845.7.
步骤4：4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯的制备Step 4: 4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) Preparation of benzyl)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000721
Figure PCTCN2022088560-appb-000721
将4-(2-(1-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯(200mg,0.236mmol)溶解在乙醇(30mL)中，加入Raney-Ni(1mL)和N 2H 4-H 2O(1mL)，室温搅拌1h，过滤，浓缩干燥得到目标产物4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯。 4-(2-(1-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tri Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate benzyl ester (200mg, 0.236 mmol) was dissolved in ethanol (30 mL), Raney-Ni (1 mL) and N 2 H 4 -H 2 O (1 mL) were added, stirred at room temperature for 1 h, filtered, concentrated and dried to obtain the target product 4-(2-(1- ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝815.4. LC-MS: (ESI, m/z): [M+H] + = 815.4.
步骤5：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌啶-1-基)甲酮的制备Step 5: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-yl)ethyl)piperidin-1-yl)methanone
Figure PCTCN2022088560-appb-000722
Figure PCTCN2022088560-appb-000722
将4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羧酸苄酯(160mg,0.196mmol)溶解在乙酸乙酯(20mL)中，加入Pd(OH) 2(32mg，20％)，60℃搅拌2h，过滤，浓缩干燥得到目标产物((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌啶-1-基)甲酮。 4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carboxylate benzyl ester (160 mg, 0.196 mmol) was dissolved in ethyl acetate (20 mL), added Pd(OH) 2 (32 mg, 20%), stirred at 60 °C for 2 h, filtered, concentrated and dried to obtain the target product ((1R,4R)-4-(4-( ((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl) (4-(2-(Piperidin-4-yl)ethyl)piperidin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝681.2. LC-MS: (ESI, m/z): [M+H] + = 681.2.
步骤6：1-(5-(4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1- Preparation of carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000723
Figure PCTCN2022088560-appb-000723
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基)乙基)哌啶-1-基)甲酮(120mg,0.176mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(84.25mg,0.194mmol)用DMSO(5mL)溶解，DIEA(68.30mg,0.529mmol)加入，反应液室温搅拌2小时，水(50mL)加入到反应液中，搅拌2分钟，过滤，固体通过反相制备纯化得到目标产物1-(5-(4-(2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-yl)ethyl)piperidin-1-yl)methanone (120 mg, 0.176 mmol) and 4-chloro - Pentafluorophenyl 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (84.25 mg, 0.194 mmol) was dissolved in DMSO (5 mL), DIEA (68.30 mg, 0.529 mmol) ) was added, the reaction solution was stirred at room temperature for 2 hours, water (50 mL) was added to the reaction solution, stirred for 2 minutes, filtered, and the solid was purified by reverse-phase preparation to obtain the target product 1-(5-(4-(2-(1-( (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methyl quinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H ,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝931.3. LC-MS: (ESI, m/z): [M+H] + = 931.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.20-8.03(m,2H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.7Hz,1H),7.41–7.34(m,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.65–5.49(m,3H),4.54-4.34(m,2H),3.98-3.85(m,4H),3.80-3.70(m,1H),3.67-3.53(m,2H),3.10-2.86(m,3H),2.80-2.60(m,4H),2.36(s,3H),1.90–1.36(m,17H),1.35-1.18(m,5H),1.16-0.86(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 8.20-8.03(m, 2H), 7.63(d, J=8.2Hz, 1H), 7.54(d, J=1.7Hz, 1H), 7.41–7.34(m, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65–5.49(m, 3H), 4.54 -4.34(m, 2H), 3.98-3.85(m, 4H), 3.80-3.70(m, 1H), 3.67-3.53(m, 2H), 3.10-2.86(m, 3H), 2.80-2.60(m, 4H), 2.36(s, 3H), 1.90-1.36(m, 17H), 1.35-1.18(m, 5H), 1.16-0.86(m, 4H).
实施例16：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 16: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoro) Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3 -Azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：1-(2-氟-3-(三氟甲基)苯基)乙烷-1-酮的制备Step 1: Preparation of 1-(2-fluoro-3-(trifluoromethyl)phenyl)ethan-1-one
Figure PCTCN2022088560-appb-000724
Figure PCTCN2022088560-appb-000724
将1-溴-2-氟-3-(三氟甲基)苯(4.0g,16.4mmol),Pd(PPh 3) 2Cl 2(1.1g,1.6mmol)，TEA(4.9g,48.9mmol)和三丁基(1-乙氧基乙烯基)锡烷(8.8g,24.4mmol)在二氧六环(80.0mL)中的反应液于80℃搅拌反应16.0h。反应用冰水(200mL)淬灭，EA(80mL×3)萃取，合并有机相并用食盐水洗，无水硫酸钠干燥，过滤，浓缩。残余物在6N HCl(20mL)中搅拌，滤液减压浓缩，粗品经柱层析(EA/PE,0-40％)纯化得到目标产物1-(2-氟-3-(三氟甲基)苯基)乙烷-1-酮。 1-Bromo-2-fluoro-3-(trifluoromethyl)benzene (4.0 g, 16.4 mmol), Pd(PPh 3 ) 2 Cl 2 (1.1 g, 1.6 mmol), TEA (4.9 g, 48.9 mmol) The reaction solution of tributyl(1-ethoxyvinyl)stannane (8.8 g, 24.4 mmol) in dioxane (80.0 mL) was stirred at 80° C. for 16.0 h. The reaction was quenched with ice water (200 mL), extracted with EA (80 mL×3), the organic phases were combined and washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was stirred in 6N HCl (20 mL), the filtrate was concentrated under reduced pressure, and the crude product was purified by column chromatography (EA/PE, 0-40%) to give the desired product 1-(2-fluoro-3-(trifluoromethyl)) phenyl)ethan-1-one.
步骤2：(S,E)-N-(1-(2-氟-3-(三氟甲基)苯基)亚乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 2: Preparation of (S,E)-N-(1-(2-fluoro-3-(trifluoromethyl)phenyl)ethylene)-2-methylpropane-2-sulfinamide
Figure PCTCN2022088560-appb-000725
Figure PCTCN2022088560-appb-000725
1-(2-氟-3-(三氟甲基)苯基)乙烷-1-酮(2.0g,9.7mmol)，Ti(OEt) 4(5.5g,24.2mmol)和(S)-丙烷-2-亚磺酰胺(1.7g,14.5mmol)在THF(40.0mL)溶液中的反应混合物于60℃下搅拌反应2h。用水(100mL)淬灭反应，并用EA(80mL×3)萃取溶液。收集有机层并用无水硫酸钠干燥，过滤并在减压下浓缩。浓缩物经柱层析纯化得到目标产物(S,E)-N-(1-(2-氟-3-(三氟甲基)苯基)亚乙基)-2-甲基丙烷-2-亚磺酰胺。 1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethan-1-one (2.0 g, 9.7 mmol), Ti(OEt) 4 (5.5 g, 24.2 mmol) and (S)-propane The reaction mixture of -2-sulfinamide (1.7 g, 14.5 mmol) in THF (40.0 mL) was stirred at 60 °C for 2 h. The reaction was quenched with water (100 mL) and the solution was extracted with EA (80 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography to obtain the target product (S,E)-N-(1-(2-fluoro-3-(trifluoromethyl)phenyl)ethylene)-2-methylpropane-2- Sulfenamide.
LC-MS:(ESI,m/z):[M+H] +＝310.2. LC-MS: (ESI, m/z): [M+H] + = 310.2.
步骤3：(S)-N-((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)-2-甲基丙烷-2-亚磺酰胺的制备Step 3: Preparation of (S)-N-((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide
Figure PCTCN2022088560-appb-000726
Figure PCTCN2022088560-appb-000726
-78℃时向(S,E)-N-(1-(2-氟-3-(三氟甲基)苯基)亚乙基)-2-甲基丙烷-2-亚磺酰胺(2.0g,6.4mmol)的THF(20.0mL)溶液中加入L-Selectride(1.0mol/L/THF,7.1mL)，反应混合物于-78℃下搅拌反应50min。用冰水(100mL)淬灭反应，并用EA(80mL×3)萃取溶液。收集有机层并用无水硫酸钠干燥，过滤并在减压下浓缩。浓缩物经柱层析(EA/PE,0-60％)纯化得到目标产物(S)-N-((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)-2-甲基丙烷-2-亚磺酰胺。To (S,E)-N-(1-(2-fluoro-3-(trifluoromethyl)phenyl)ethylene)-2-methylpropane-2-sulfinamide (2.0 g, 6.4 mmol) in THF (20.0 mL) solution was added L-Selectride (1.0 mol/L/THF, 7.1 mL), and the reaction mixture was stirred at -78 °C for 50 min. The reaction was quenched with ice water (100 mL), and the solution was extracted with EA (80 mL x 3). The organic layer was collected and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by column chromatography (EA/PE, 0-60%) to obtain the target product (S)-N-((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl yl)-2-methylpropane-2-sulfinamide.
LC-MS:(ESI,m/z):[M+H] +＝312.2. LC-MS: (ESI, m/z): [M+H] + = 312.2.
1H NMR(400MHz,CDCl 3)δ7.65-7.59(m,1H),7.57-7.51(m,1H),7.27-7.22(m,1H),4.91–4.81(m,1H),3.55(d,J＝5.2Hz,1H),1.56(d,J＝6.7Hz,3H),1.23(s,9H). 1 H NMR (400 MHz, CDCl 3 ) δ 7.65-7.59 (m, 1H), 7.57-7.51 (m, 1H), 7.27-7.22 (m, 1H), 4.91-4.81 (m, 1H), 3.55 (d , J=5.2Hz, 1H), 1.56(d, J=6.7Hz, 3H), 1.23(s, 9H).
步骤4：(R)-1-(2-氟-3-(三氟甲基)苯基)乙烷-1-胺盐酸盐的制备Step 4: Preparation of (R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethane-1-amine hydrochloride
Figure PCTCN2022088560-appb-000727
Figure PCTCN2022088560-appb-000727
将(S)-N-((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)-2-甲基丙烷-2-亚磺酰胺(2.0g,3.2mmol)的盐酸二氧六环(4N,20.0mL)反应混合物于25℃下搅拌反应1.0h。反应液减压下浓缩。浓缩物经PE(20mL×3)洗涤得到目标产物(R)-1-(2-氟-3-(三氟甲基)苯基)乙烷-1-胺盐酸盐。(S)-N-((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide (2.0 g, 3.2 mmol) in dioxane hydrochloride (4N, 20.0 mL) and the reaction mixture was stirred at 25 °C for 1.0 h. The reaction solution was concentrated under reduced pressure. The concentrate was washed with PE (20 mL×3) to obtain the target product (R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethane-1-amine hydrochloride.
LC-MS:(ESI,m/z):[M+H] +＝208.1. LC-MS: (ESI, m/z): [M+H] + = 208.1.
步骤5：(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 5: (1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- Preparation of methyl 2-methylquinazolin-6-yl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000728
Figure PCTCN2022088560-appb-000728
将(R)-1-(2-氟-3-(三氟甲基)苯基)乙烷-1-胺(0.7g,3.3mmol)，DIEA(928.8mg,7.2mmol)和(1R,4R)-4-(4-氯-7-甲氧基-2-甲基喹唑啉-6-基)环己基-1-羧酸甲酯(835mg,2.4mmol)在二氧六环(10.0mL)中的反应混合物于110℃下搅拌反应20.0h。加水(50mL)淬灭反应，EA(30.0mL×2)萃取，合并有机相并用食盐水洗，无水硫酸钠干燥，有机相减压下浓缩。浓缩物经制备HPLC(乙腈/0.05％HCOOH水溶液,5％至95％)纯化得到目标产物(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。Combine (R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethane-1-amine (0.7 g, 3.3 mmol), DIEA (928.8 mg, 7.2 mmol) and (1R,4R) )-4-(4-chloro-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl-1-carboxylate (835 mg, 2.4 mmol) in dioxane (10.0 mL) ) was stirred at 110 °C for 20.0 h. Water (50 mL) was added to quench the reaction, EA (30.0 mL×2) was extracted, the organic phases were combined and washed with brine, dried over anhydrous sodium sulfate, and the organic phase was concentrated under reduced pressure. The concentrate was purified by preparative HPLC (acetonitrile/0.05% aqueous HCOOH, 5% to 95%) to give the desired product (1R,4R)-4-(4-(((R)-1-(2-fluoro-3-( Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝520.3. LC-MS: (ESI, m/z): [M+H] + = 520.3.
步骤6：(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 6: (1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- Preparation of 2-Methylquinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000729
Figure PCTCN2022088560-appb-000729
将(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(100mg,0.2mmol)，LiOH(48mg,2.0mmol)在THF/H 2O(2.0mL/1.0mL)中的反应混合物于50℃下搅拌反应12.0h。反应液用1N HCl调节pH为4-5，减压浓缩得到目标产物(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 (1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Reaction of methylquinazolin-6-yl)cyclohexane-1-carboxylate (100 mg, 0.2 mmol), LiOH (48 mg, 2.0 mmol) in THF/H 2 O (2.0 mL/1.0 mL) The mixture was stirred at 50 °C for 12.0 h. The pH of the reaction solution was adjusted to 4-5 with 1N HCl, and concentrated under reduced pressure to obtain the target product (1R,4R)-4-(((R)-1-(2-fluoro-3-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝506.4. LC-MS: (ESI, m/z): [M+H] + = 506.4.
步骤7：4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己 烷-1-羰基)哌嗪-1-羧酸叔丁酯的制备Step 7: 4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methyl Preparation of tert-butyl oxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000730
Figure PCTCN2022088560-appb-000730
向(1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(110mg,0.2mmol)，哌嗪-1-羧酸叔丁酯(45mg,0.22mmol)和DIEA(85mg,0.6mmol)在DMF(2mL)的溶液中加入HATU(124mg,0.24mmol)，反应混合物于室温下搅拌反应2h。反应用冰水(20mL)淬灭，过滤收集析出物，然后真空干燥得到目标产物4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯。To (1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (110 mg, 0.2 mmol), piperazine-1-carboxylic acid tert-butyl ester (45 mg, 0.22 mmol) and DIEA (85 mg, 0.6 mmol) in HATU (124 mg, 0.24 mmol) was added to the solution of DMF (2 mL), and the reaction mixture was stirred at room temperature for 2 h. The reaction was quenched with ice water (20 mL), the precipitate was collected by filtration, and then dried in vacuo to obtain the target product 4-((1R,4R)-4-(4-((((R)-1-(2-fluoro-3- (Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝674.5. LC-MS: (ESI, m/z): [M+H] + = 674.5.
步骤8：((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮的制备Step 8: ((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Preparation of -2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000731
Figure PCTCN2022088560-appb-000731
将4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯(110mg,0.1mmol)在TFA/DCM(1mL/3mL)中的反应混合物于室温下搅拌反应1.0h。反应液减压浓缩得到目标产物((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮。4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Reaction mixture of tert-butyl 2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate (110 mg, 0.1 mmol) in TFA/DCM (1 mL/3 mL) The reaction was stirred at room temperature for 1.0 h. The reaction solution was concentrated under reduced pressure to obtain the target product ((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝574.2. LC-MS: (ESI, m/z): [M+H] + = 574.2.
步骤9：9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 9: 9-((4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan- Preparation of tert-butyl 3-carboxylate
Figure PCTCN2022088560-appb-000732
Figure PCTCN2022088560-appb-000732
向((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(60mg,0.1mmol)和9-甲醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(35mg,0.12mmol)的THF(5.0mL)溶液中加入STAB(64mg,0.3mmol)，然后反应混合物于室温下搅拌反应2.0h。加冰水(10mL)淬灭反应，EA(30.0mL×2)萃取，合并有机相并用食盐水洗，无水硫酸钠干燥，减压浓缩。浓缩物经柱层析(MeOH/DCM,0-10％)纯化得到目标产物9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。To ((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone (60 mg, 0.1 mmol) and 9-carbaldehyde-3-azaspiro[5.5]undecan-3-carboxy To a solution of tert-butyl acid (35 mg, 0.12 mmol) in THF (5.0 mL) was added STAB (64 mg, 0.3 mmol), and the reaction mixture was stirred at room temperature for 2.0 h. Add ice water (10 mL) to quench the reaction, extract with EA (30.0 mL×2), combine the organic phases, wash with brine, dry over anhydrous sodium sulfate, and concentrate under reduced pressure. The concentrate was purified by column chromatography (MeOH/DCM, 0-10%) to give the target product 9-((4-((1R,4R)-4-(4-((((R)-1-(2-fluoro) -3-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl-1-carbonyl)piperazin-1-yl) Methyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝839.4. LC-MS: (ESI, m/z): [M+H] + = 839.4.
步骤10：(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮的制备Step 10: (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R )-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone preparation
Figure PCTCN2022088560-appb-000733
Figure PCTCN2022088560-appb-000733
将9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷 -1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(70mg,0.08mmol)在TFA/DCM(1mL/3mL)中的反应混合物于室温下搅拌反应1.0h。反应液直接浓缩得到目标产物(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮。9-((4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- The reaction mixture of tert-butyl carboxylate (70 mg, 0.08 mmol) in TFA/DCM (1 mL/3 mL) was stirred at room temperature for 1.0 h. The reaction solution was directly concentrated to obtain the target product (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4- (((R)-1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl ) ketone.
LC-MS:(ESI,m/z):[M+H] +＝739.5. LC-MS: (ESI, m/z): [M+H] + = 739.5.
步骤11：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Step 11: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(2-fluoro-3-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3- Azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000734
Figure PCTCN2022088560-appb-000734
向(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(60mg,0.08mmol)的DMSO(1.0mL)溶液中加入DIEA(31mg,0.24mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(43mg,0.1mmol)，然后反应混合物于室温下搅拌反应2.0h。反应用水(15mL)淬灭，EA(30mL×2)萃取，合并有机相并用食盐水洗，干燥，减压浓缩。浓缩物经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得到目标产物1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(2-氟-3-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)- 1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone (60 mg, 0.08 mmol) in DMSO (1.0 mL) was added DIEA (31 mg, 0.24 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluoro Phenyl ester (43 mg, 0.1 mmol), then the reaction mixture was stirred at room temperature for 2.0 h. The reaction was quenched with water (15 mL), extracted with EA (30 mL×2), the organic phases were combined and washed with brine, dried and concentrated under reduced pressure. The concentrate was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(2-chloro-5-(9-((4-((1R,4R)-4 -(4-(((R)-1-(2-Fluoro-3-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline-6- yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H, 3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝989.4. LC-MS: (ESI, m/z): [M+H] + = 989.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.26(s,1H),8.10(s,1H),7.80(s,1H),7.63(d,J＝7.5Hz,2H),7.55(s,1H),7.42–7.34(m,2H),6.99(s,1H),5.77(s,1H),3.88(s,3H),3.82-3.72(m,1H),3.68-3.42(m,7H),3.02-2.92(m,1H),2.78-2.70(m,2H),2.70-2.63(m,1H),2.38-2.25(m,7H),2.18-2.10(m,2H),1.90-1.78(m,4H),1.71-1.22(m,18H),1.98-1.00(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s, 1H), 8.26(s, 1H), 8.10(s, 1H), 7.80(s, 1H), 7.63(d, J=7.5Hz, 2H), 7.55(s, 1H), 7.42–7.34(m, 2H), 6.99(s, 1H), 5.77(s, 1H), 3.88(s, 3H), 3.82-3.72(m, 1H), 3.68 -3.42(m, 7H), 3.02-2.92(m, 1H), 2.78-2.70(m, 2H), 2.70-2.63(m, 1H), 2.38-2.25(m, 7H), 2.18-2.10(m, 2H), 1.90-1.78(m, 4H), 1.71-1.22(m, 18H), 1.98-1.00(m, 4H).
实施例17：N-(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)乙酰胺Example 17: N-(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7- Methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)acetamide
Figure PCTCN2022088560-appb-000735
Figure PCTCN2022088560-appb-000735
将1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮(70mg,0.07mmol)的乙酸酐(3.0mL)反应混合物于室温下搅拌反应12.0h。反应液直接减压浓缩。浓缩物经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得到目标产物N-(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)乙酰胺。 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione (70 mg, 0.07 mmol) in acetic anhydride (3.0 mL) The reaction mixture was stirred at room temperature 12.0h. The reaction solution was directly concentrated under reduced pressure. The concentrate was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product N-(3-((R)-1-((6-((1R,4R)-4 -(4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane Alk-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl) group) phenyl) acetamide.
LC-MS:(ESI,m/z):[M+H] +＝1028.3. LC-MS: (ESI, m/z): [M+H] + = 1028.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),10.22(s,1H),8.19(d,J＝7.3Hz,1H),8.06(s,1H),7.96(s,1H),7.78(s,1H),7.63(d,J＝8.1Hz,1H),7.54(s,1H),7.47(s,1H),7.38(d,J＝7.9Hz,1H),7.00(s,1H),5.68–5.54(m,1H),3.88(s,3H),3.79-3.72(m,1H),3.62-3.41(m,7H),2.98-2.91(m,1H),2.78-2.70(m,2H),2.70-2.63(m,1H),2.38-2.22(m,7H),2.18-2.08(m,2H),2.03(s,3H),1.89-1.78(m,4H),1.74–1.22(m,18H),1.18-0.98(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 10.22(s, 1H), 8.19(d, J=7.3Hz, 1H), 8.06(s, 1H), 7.96(s, 1H), 7.78(s, 1H), 7.63(d, J=8.1Hz, 1H), 7.54(s, 1H), 7.47(s, 1H), 7.38(d, J=7.9Hz, 1H), 7.00( s, 1H), 5.68-5.54(m, 1H), 3.88(s, 3H), 3.79-3.72(m, 1H), 3.62-3.41(m, 7H), 2.98-2.91(m, 1H), 2.78- 2.70(m, 2H), 2.70-2.63(m, 1H), 2.38-2.22(m, 7H), 2.18-2.08(m, 2H), 2.03(s, 3H), 1.89-1.78(m, 4H), 1.74-1.22(m,18H),1.18-0.98(m,4H).
实施例18：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(异丙基氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶- 2,4(1H,3H)-二酮Example 18: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(isopropylamino)- 5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl) Methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000736
Figure PCTCN2022088560-appb-000736
0℃时向1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮(70mg,0.07mmol)，丙酮(40mg,0.7mmol)和AcOH(0.2mL)的MeOH/THF(1.0mL/1.0mL)溶液中加入STAB(89mg,0.42mmol)。然后反应混合物于室温下搅拌反应30h。反应加水淬灭，EA萃取，合并有机相并用食盐水洗，无水硫酸钠干燥，减压浓缩。浓缩物经制备HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％至95％)纯化得到目标产物1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(异丙基氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)benzene)) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione (70 mg, 0.07 mmol), acetone (40 mg, 0.7 mmol) and AcOH ( To a solution of 0.2 mL) in MeOH/THF (1.0 mL/1.0 mL) was added STAB (89 mg, 0.42 mmol). The reaction mixture was then stirred at room temperature for 30 h. The reaction was quenched by adding water, extracted with EA, and the organic phases were combined and washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The concentrate was purified by preparative HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 % to 95%) to give the desired product 1-(2-chloro-5-(9-((4-((1R,4R)-4 -(4-(((R)-1-(3-(isopropylamino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2 ,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1028.3. LC-MS: (ESI, m/z): [M+H] + = 1028.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),10.22(s,1H),8.19(d,J＝7.3Hz,1H),8.06(s,1H),7.96(s,1H),7.78(s,1H),7.63(d,J＝8.1Hz,1H),7.54(s,1H),7.47(s,1H),7.38(d,J＝7.9Hz,1H),7.00(s,1H),5.68–5.54(m,1H),3.88(s,3H),3.82-3.56(m,8H),2.98-2.91(m,1H),2.78-2.70(m,2H),2.70-2.63(m,2H),2.38-2.22(m,7H),2.18-2.08(m,2H),1.95-1.75(m,4H),1.89-1.48(m,15H),1.42–1.25(m,6H),1.18-0.98(m,7H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 10.22(s, 1H), 8.19(d, J=7.3Hz, 1H), 8.06(s, 1H), 7.96(s, 1H), 7.78(s, 1H), 7.63(d, J=8.1Hz, 1H), 7.54(s, 1H), 7.47(s, 1H), 7.38(d, J=7.9Hz, 1H), 7.00( s, 1H), 5.68-5.54(m, 1H), 3.88(s, 3H), 3.82-3.56(m, 8H), 2.98-2.91(m, 1H), 2.78-2.70(m, 2H), 2.70- 2.63(m, 2H), 2.38-2.22(m, 7H), 2.18-2.08(m, 2H), 1.95-1.75(m, 4H), 1.89-1.48(m, 15H), 1.42–1.25(m, 6H) ),1.18-0.98(m,7H).
实施例19：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 19: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl )piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-((2-(1-(叔丁氧羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000737
Figure PCTCN2022088560-appb-000737
将4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(1.9g,5.81mmol)和氯甲酸苄酯(1.19mg,6.97mmol)的ACN/sat.NaHCO 3(30mL/30mL)反应液室温下搅拌过夜。反应液加水淬灭(50mL)，然后用EA萃取(50mL×3)。有机相用饱和食盐水洗，Na 2SO 4干燥，减压浓缩。粗产品经flash柱(EA:PE＝0～7:3)纯化得到目标产物4-((2-(1-(叔丁氧羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯。 A mixture of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate (1.9 g, 5.81 mmol) and benzyl chloroformate (1.19 mg, 6.97 mmol) The ACN/ sat.NaHCO3 (30 mL/30 mL) reaction was stirred at room temperature overnight. The reaction solution was quenched with water (50 mL), and then extracted with EA (50 mL×3). The organic phase was washed with saturated brine, dried over Na 2 SO 4 and concentrated under reduced pressure. The crude product was purified by flash column (EA:PE=0～7:3) to obtain the target product 4-((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethoxy)methyl)piperidine Benzyl pyridine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝461.3. LC-MS: (ESI, m/z): [M+H] + = 461.3.
步骤2：4-((2-哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯的制备Step 2: Preparation of benzyl 4-((2-piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000738
Figure PCTCN2022088560-appb-000738
向4-((2-(1-(叔丁氧羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯(600mg,1.3mmol)的DCM(5mL)溶液中加入TFA(2mL)。反应液室温下搅拌2h。反应液直接减压浓缩得到目标产物4-((2-哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯。所得粗产物无需纯化直接用于下一步反应。To benzyl 4-((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate (600 mg, 1.3 mmol) in DCM (5 mL) To the solution was added TFA (2 mL). The reaction solution was stirred at room temperature for 2h. The reaction solution was directly concentrated under reduced pressure to obtain the target product, benzyl 4-((2-piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate. The obtained crude product was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝361.1. LC-MS: (ESI, m/z): [M+H] + = 361.1.
步骤3：(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 3: (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl) preparation of cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000739
Figure PCTCN2022088560-appb-000739
将(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(21mg,0.34mmol),LiOH(71mg,1.70mmol)的THF/H 2O(8mL/4mL)反应液在50℃下搅拌过夜。反应液加入10％的柠檬酸水溶液(5mL)，用EA(20mL×3)萃取。有机相用饱和食盐水洗涤(100mL)，Na 2SO 4干燥，过滤，减压浓缩得到目标产物(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- Methyl 7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate (21 mg, 0.34 mmol), LiOH (71 mg, 1.70 mmol) in THF/H 2 O (8 mL) /4mL) The reaction solution was stirred at 50°C overnight. The reaction solution was added with 10% aqueous citric acid solution (5 mL), and extracted with EA (20 mL×3). The organic phase was washed with saturated brine (100 mL), dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure to obtain the target product (1R,4R)-4-(4-(((R)-1-(3-((tert. Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid .
LC-MS:(ESI,m/z):[M+H] +＝603.1. LC-MS: (ESI, m/z): [M+H] + = 603.1.
步骤4：4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-(叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯的制备Step 4: 4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-(tert-butoxycarbonyl)amino)-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl ) Preparation of benzyl piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000740
Figure PCTCN2022088560-appb-000740
向((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(200mg,0.33mmol)的DMF(10mL)溶液中加入4-((2-哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯(155mg,0.43mmol)，HATU(190mg,0.50mmol)和DIEA(128mg,0.99mmol)。反应混合液在室温下搅拌2h。反应液加入水(100mL)，用EA(30mL×3)萃取。有机相用饱和食盐水洗涤(100mL)，Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(EA:PE＝0～4:1)纯化得到目标产物4-((2-(1R,4R)-4-(4-(((R)-1-(3-(叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯。 To ((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (200 mg, 0.33 mmol) in DMF (10 mL) was added 4-((2-piperidine- 4-yl)ethoxy)methyl)piperidine-1-carboxylate benzyl ester (155 mg, 0.43 mmol), HATU (190 mg, 0.50 mmol) and DIEA (128 mg, 0.99 mmol). The reaction mixture was stirred at room temperature for 2 h. The reaction solution was added with water (100 mL) and extracted with EA (30 mL×3). The organic phase was washed with saturated brine (100 mL), dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～4:1) to obtain the target product 4-((2-(1R,4R)-4-(4-((((R)-1-(3-(tert. Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl) Benzyl piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝945.3. LC-MS: (ESI, m/z): [M+H] + = 945.3.
步骤5：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 5: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidin-4-yl Preparation of methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester
Figure PCTCN2022088560-appb-000741
Figure PCTCN2022088560-appb-000741
向4-((2-(1R,4R)-4-(4-(((R)-1-(3-(叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯(230mg,0.24mmol)的EA(20mL)溶液中加入Pd(OH) 2/C(100mg)。反应混合液在70℃下搅拌过夜。反应液经硅藻土过滤，滤液减压浓缩得到目标产物(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。所得产物无需纯化直接用于下一步反应。 To 4-((2-(1R,4R)-4-(4-(((R)-1-(3-(tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1- To a solution of benzyl carboxylate (230 mg, 0.24 mmol) in EA (20 mL) was added Pd(OH) 2 /C (100 mg). The reaction mixture was stirred at 70°C overnight. The reaction solution was filtered through celite, and the filtrate was concentrated under reduced pressure to obtain the target product (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-( 4-(2-(Piperidin-4-ylmethoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl) ) phenyl) tert-butyl carbamate. The obtained product was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝811.3. LC-MS: (ESI, m/z): [M+H] + = 811.3.
步骤6：(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 6: (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-Chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2- Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000742
Figure PCTCN2022088560-appb-000742
将(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(200mg,0.24mmol)，4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(126mg,0.29mmol)和DIEA(93mg,0.72mmol)的DMSO(5mL)溶液在室温下搅拌过夜。反应液用水(50mL)稀释，然后用DCM(20mL×2)萃取。合并有机相并用饱和食盐水洗涤，经干燥，过滤并减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到目标产物(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。(3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidin-4-ylmethoxy (yl)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (200mg, 0.24mmol) ), pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (126 mg, 0.29 mmol) and DIEA (93 mg, 0.72 mmol) in DMSO (5 mL) The solution was stirred at room temperature overnight. The reaction solution was diluted with water (50 mL), and then extracted with DCM (20 mL×2). The organic phases were combined and washed with saturated brine, dried, filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain the target product (3-((R)-1-((6-((1R,4R)-4-(4-(2-( (1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine -1-Carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1061.3. LC-MS: (ESI, m/z): [M+H] + = 1061.3.
步骤7：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl) Preparation of piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000743
Figure PCTCN2022088560-appb-000743
向(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的DCM(3mL)溶液中滴加TFA(1.0mL)。反应液在室温下搅拌2h。反应液中加入DIEA(5mL)，然后加水(50mL)稀释，DCM(30mL×3)萃取。有机相用饱和食盐水(100mL)洗涤,Na 2SO 4干燥，过滤，减压浓缩。粗产品经Pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到目标产物1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-chloro-3-(2,4-dioxo) Tetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl To a solution of tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate in DCM (3 mL) was added TFA (1.0 mL) dropwise. The reaction solution was stirred at room temperature for 2 h. DIEA (5 mL) was added to the reaction solution, then diluted with water (50 mL), and extracted with DCM (30 mL×3). The organic phase was washed with saturated brine (100 mL), dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure. The crude product was purified by Pre-HPLC (CH 3 CN/0.08% NH 4 HCO 3 aqueous solution, 5%~95%) to obtain the target product 1-(5-(4-((2-(1-((1R,4R) -4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H, 3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝961.1. LC-MS: (ESI, m/z): [M+H] + = 961.1.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),9.32(s,1H),8.25(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.8Hz,1H),7.37(dd,J＝8.2,1.8Hz,1H),7.04(s,1H),6.86(d,J＝7.3Hz,2H),6.74(s,1H),5.75-5.55(m,3H),4.50-4.30(m,2H),3.98-3.87(m,4H),3.80-3.70(m,1H),3.68-3.54(m,2H),3.41(t,J＝6.2Hz,2H),3.23(d,J＝6.0Hz,2H),3.12-2.90(m,3H),2.82-2.60(m,4H),1.92-1.40(m,22H),1.12-0.92(m,5H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 9.32(s, 1H), 8.25(s, 1H), 7.63(d, J=8.2Hz, 1H), 7.54(d, J=1.8Hz, 1H), 7.37(dd, J=8.2, 1.8Hz, 1H), 7.04(s, 1H), 6.86(d, J=7.3Hz, 2H), 6.74(s, 1H), 5.75- 5.55(m, 3H), 4.50-4.30(m, 2H), 3.98-3.87(m, 4H), 3.80-3.70(m, 1H), 3.68-3.54(m, 2H), 3.41(t, J=6.2 Hz, 2H), 3.23(d, J＝6.0Hz, 2H), 3.12-2.90(m, 3H), 2.82-2.60(m, 4H), 1.92-1.40(m, 22H), 1.12-0.92(m, 5H).
实施例20：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 20: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000744
Figure PCTCN2022088560-appb-000744
(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮(200mg,0.12mmol),3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯(62mg,0.15mmol)和DIEA(77mg,0.60mmol)在DMSO(5mL)中的反应液，室温下搅拌过夜。反应液用水(50mL)稀释。然后用DCM(20mL×3)。有机相用饱和食盐水(60mL)洗涤，Na 2SO 4干燥，过滤，减压浓缩。所得粗品经薄层制备板纯化(DCM:MeOH＝10:1)得到目标产物1-(5-(9-((4-((1R,4R)- 4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)-1 -(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane)methanone (200 mg, 0.12 mmol), 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester (62 mg, 0.15 mmol) and DIEA (77 mg, 0.60 mmol) in DMSO (5 mL) and stirred overnight at room temperature. The reaction solution was diluted with water (50 mL). Then DCM (20 mL x 3). The organic phase was washed with saturated brine (60 mL), dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by thin-layer preparative plate (DCM:MeOH=10:1) to obtain the target product 1-(5-(9-((4-((1R,4R)- 4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl) Piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dihydropyrimidine ketone.
LC-MS:(ESI,m/z):[M+H] +＝982.2. LC-MS: (ESI, m/z): [M+H] + = 982.2.
1H NMR(400MHz,DMSO-d 6)δ10.33(s,1H),8.14–8.02(m,2H),7.36(dd,J＝8.4,2.1Hz,1H),7.32(d,J＝2.1Hz,1H),7.15(d,J＝8.7Hz,1H),6.99(s,1H),6.87(s,1H),6.85(s,1H),6.70(s,1H),5.62–5.49(m,3H),3.88(s,3H),3.84(s,3H),3.59(t,J＝6.7Hz,2H),3.52-3.42(m,6H),3.02-2.92(m,1H),2.70-2.68(m,3H),2.40-2.24(m,7H),2.16-2.06(m,2H),1.90-1.75(m,4H),1.78-1.40(m,14H),1.32-1.22(m,4H),1.12-0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.33 (s, 1H), 8.14-8.02 (m, 2H), 7.36 (dd, J=8.4, 2.1 Hz, 1H), 7.32 (d, J=2.1 Hz, 1H), 7.15(d, J=8.7Hz, 1H), 6.99(s, 1H), 6.87(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.62–5.49(m ,3H),3.88(s,3H),3.84(s,3H),3.59(t,J=6.7Hz,2H),3.52-3.42(m,6H),3.02-2.92(m,1H),2.70- 2.68(m, 3H), 2.40-2.24(m, 7H), 2.16-2.06(m, 2H), 1.90-1.75(m, 4H), 1.78-1.40(m, 14H), 1.32-1.22(m, 4H) ),1.12-0.92(m,4H).
实施例21：1-(3-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 21: 1-(3-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000745
Figure PCTCN2022088560-appb-000745
(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(200mg,0.12mmol),3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(60mg,0.15mmol)和DIEA(77mg,0.60mmol)在DMSO(5mL)中的反应液，室温下搅拌过夜。反应液用水(50mL)稀释。然后用DCM(20mL×3)萃取。有机相用饱和食盐水(60mL)洗涤，Na 2SO 4干燥，过滤，减压浓缩。所得粗品先经柱层析(MeOH/DCM＝0～1:9)纯化，再经薄层制备板纯化(DCM:MeOH＝10:1)得到目标产物1-(3-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)-1 -(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone (200 mg, 0.12 mmol), pentafluorophenyl 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (60 mg, 0.15 mmol) and DIEA (77 mg, 0.60 mmol) in DMSO (5 mL) The reaction solution was stirred at room temperature overnight. The reaction solution was diluted with water (50 mL). It was then extracted with DCM (20 mL x 3). The organic phase was washed with saturated brine (60 mL), dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was first purified by column chromatography (MeOH/DCM=0～1:9), and then purified by thin-layer preparative plate (DCM:MeOH=10:1) to obtain the target product 1-(3-(9-((4 -((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)di Hydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝952.5. LC-MS: (ESI, m/z): [M+H] + = 952.5.
1H NMR(400MHz,DMSO-d 6)δ10.41(s,1H),8.20-8.04(m,2H),7.47-7.34(m,3H),7.22(d,J＝7.4Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.63–5.48(m,3H),3.88(s,3H),3.82(t,J＝6.7Hz,2H),3.62-3.50(m,2H),3.50-3.40(m,4H),3.02-2.90(m,1H),2.71(t,J＝6.6Hz,2H),2.68-2.60(m,1H),2.40-2.30(m,5H),2.20-2.10(m,2H),1.90-1.80(m,4H),1.68-1.40(m,18H),1.11-0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.41(s, 1H), 8.20-8.04(m, 2H), 7.47-7.34(m, 3H), 7.22(d, J=7.4Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.63–5.48(m, 3H), 3.88(s, 3H), 3.82(t, J= 6.7Hz, 2H), 3.62-3.50(m, 2H), 3.50-3.40(m, 4H), 3.02-2.90(m, 1H), 2.71(t, J＝6.6Hz, 2H), 2.68-2.60(m ,1H),2.40-2.30(m,5H),2.20-2.10(m,2H),1.90-1.80(m,4H),1.68-1.40(m,18H),1.11-0.92(m,4H).
实施例22：1-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 22: 1-(4-(9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)benzene)) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000746
Figure PCTCN2022088560-appb-000746
将(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(80mg,0.109mmol)和4-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(44mg,0.109mmol)用DMSO(5mL)溶解，加入DIEA(42mg,0.327mmol)，然后反应液室温搅拌2小时，水(50mL)加入到反应液中，搅拌2分钟，过滤，固体使用柱层析(10％MeOH/DCM)纯化后，再通过p-TLC(MeOH/DCM＝1/10)纯化得到1-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。(4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone (80 mg, 0.109 mmol) and pentafluorophenyl 4-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (44 mg, 0.109 mmol) were dissolved in DMSO (5 mL) and DIEA (42 mg, 0.109 mmol) was added. 0.327 mmol), then the reaction solution was stirred at room temperature for 2 hours, water (50 mL) was added to the reaction solution, stirred for 2 minutes, filtered, the solid was purified by column chromatography (10% MeOH/DCM), and then passed through p-TLC (MeOH). /DCM=1/10) to obtain 1-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(tris) Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)- 3-Azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝952.6. LC-MS: (ESI, m/z): [M+H] + = 952.6.
1H NMR(400MHz,DMSO-d 6)δ10.43(s,1H),8.09(d,J＝22.5Hz,2H),7.39(s,4H),6.99(s,1H),6.86(d,J＝10.9Hz,2H),6.70(s,1H),5.64–5.48(m,3H),3.88(s,3H),3.83(t,J＝6.5Hz,2H),3.60–3.53(m,2H),3.50–3.40(m,5H),2.94(s,1H),2.77–2.59(m,4H),2.31(d,J＝37.6Hz,8H),2.12(s,2H),1.91–1.75(m,4H),1.75–1.60(s,4H),1.60–1.40(m,11H),1.15–0.95(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.43(s, 1H), 8.09(d, J=22.5Hz, 2H), 7.39(s, 4H), 6.99(s, 1H), 6.86(d, J=10.9Hz, 2H), 6.70(s, 1H), 5.64-5.48(m, 3H), 3.88(s, 3H), 3.83(t, J=6.5Hz, 2H), 3.60-3.53(m, 2H) ), 3.50–3.40 (m, 5H), 2.94 (s, 1H), 2.77–2.59 (m, 4H), 2.31 (d, J=37.6Hz, 8H), 2.12 (s, 2H), 1.91–1.75 ( m, 4H), 1.75–1.60 (s, 4H), 1.60–1.40 (m, 11H), 1.15–0.95 (m, 4H).
实施例23：3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮Example 23: 3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)phenyl)piperidine-2,6-dione
Figure PCTCN2022088560-appb-000747
Figure PCTCN2022088560-appb-000747
将4-(2,6-二氧代基哌啶-3-基)苯甲酸五氟苯酯(143.12mg,0.358mmol)和(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷)甲酮(240mg,0.326mmol)用DMSO(5mL)溶解，加入DIEA(126.2mg,0.978mmol)，然后室温搅拌2小时，水(50mL)加入到反应液中，搅拌2分钟，过滤，固体通过反相制备纯化得到3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮。Pentafluorophenyl 4-(2,6-dioxopiperidin-3-yl)benzoate (143.12 mg, 0.358 mmol) and (4-((3-azaspiro[5.5]undecane- 9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) Ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane)methanone (240 mg, 0.326 mmol) was dissolved in DMSO (5 mL) and DIEA (126.2 mg, 0.978 mg) was added mmol), then stirred at room temperature for 2 hours, water (50 mL) was added to the reaction solution, stirred for 2 minutes, filtered, and the solid was purified by reverse-phase preparation to obtain 3-(4-(9-((4-((1R,4R) -4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexyl-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione .
LC-MS:(ESI,m/z):[M+H] +＝951.1. LC-MS: (ESI, m/z): [M+H] + = 951.1.
1H NMR(400MHz,DMSO-d 6)δ10.86(s,1H),8.20-8.10(m,1H),8.06(s,1H),7.33(d,J＝8.1Hz,2H),7.28(d,J＝8.1Hz,2H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.67-5.47(m,3H),3.94–3.88(m,4H),3.65-3.42(m,8H),3.00-2.90(m,1H),2.71–2.62(m,4H),2.42-2.22(m,10H),2.16–2.02(m,4H),1.90-1.76(m,6H),1.74-1.36(m,10H),1.20-0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.86(s, 1H), 8.20-8.10(m, 1H), 8.06(s, 1H), 7.33(d, J=8.1Hz, 2H), 7.28( d, J＝8.1Hz, 2H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.67-5.47(m, 3H), 3.94-3.88 (m,4H), 3.65-3.42(m,8H), 3.00-2.90(m,1H), 2.71-2.62(m,4H), 2.42-2.22(m,10H), 2.16-2.02(m,4H) ,1.90-1.76(m,6H),1.74-1.36(m,10H),1.20-0.92(m,4H).
实施例24：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 24: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000748
Figure PCTCN2022088560-appb-000748
将(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(100mg,0.136mmol)和3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-氟苯甲酸五氟苯酯(57mg,0.136mmol)用DMSO(5mL)溶解，加入DIEA(53mg,0.41mmol)，反应液室温搅拌2小时，用水(50mL)稀释，搅拌2分钟，过滤，固体使用柱层析(MeOH:DCM＝1:9)纯化后，再用p-TLC(MeOH:DCM＝1:10)纯化2次得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮。(4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)methanone (100 mg, 0.136 mmol) and 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoic acid pentafluorophenyl ester (57 mg, 0.136 mmol) were dissolved in DMSO (5 mL) and added DIEA (53 mg, 0.41 mmol), the reaction solution was stirred at room temperature for 2 hours, diluted with water (50 mL), stirred for 2 minutes, filtered, and the solid was purified by column chromatography (MeOH:DCM=1:9), then p-TLC ( MeOH:DCM=1:10) purified twice to give 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5) -(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methan yl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝970.7. LC-MS: (ESI, m/z): [M+H] + = 970.7.
1H NMR(400MHz,DMSO-d 6)δ10.52(s,1H),8.14-8.08(m,1H),8.06(s,1H),7.50(d,J＝7.9Hz,1H),7.37(d,J＝8.6Hz,2H),6.99(s,1H),6.89(s,1H),6.86(s,1H),6.70(s,1H),5.61–5.48(m,3H),3.88(s,3H),3.75(t,J＝6.6Hz,2H),3.64–3.53(m,2H),3.52-3.40(m,5H),3.02-2.90(m,1H),2.77–2.56(m,4H),2.38–2.21(m,8H),2.18-2.07(m,2H),1.90–1.77(m,4H),1.73-1.40(m,15H),1.13-0.96(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.52(s, 1H), 8.14-8.08(m, 1H), 8.06(s, 1H), 7.50(d, J=7.9Hz, 1H), 7.37( d, J=8.6Hz, 2H), 6.99(s, 1H), 6.89(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.61–5.48(m, 3H), 3.88(s ,3H),3.75(t,J＝6.6Hz,2H),3.64-3.53(m,2H),3.52-3.40(m,5H),3.02-2.90(m,1H),2.77-2.56(m,4H) ), 2.38-2.21(m, 8H), 2.18-2.07(m, 2H), 1.90-1.77(m, 4H), 1.73-1.40(m, 15H), 1.13-0.96(m, 4H).
实施例25：1-(5-(4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 25: 1-(5-(4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoro) Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)(methyl) yl)amino)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(((2-(1-(叔丁氧羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)(methyl)amino)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000749
Figure PCTCN2022088560-appb-000749
向4-(2-(甲氨基)乙基)哌啶-1-羧酸叔丁酯(310mg,1.28mmol)和4-甲醛哌啶-1-羧酸苄酯(316mg,1.28mmol)的THF(10mL)溶液中加入STAB(814mg,3.84mmol)。反应液在室温搅拌2h。反应液中加水(50mL)稀释，EA(50mL×3)。合并有机相并用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，浓缩。所得粗品经flash柱(MeOH/DCM＝0～1:4)得到4-(((2-(1-(叔丁氧羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯。 To tert-butyl 4-(2-(methylamino)ethyl)piperidine-1-carboxylate (310 mg, 1.28 mmol) and benzyl 4-carbaldehyde piperidine-1-carboxylate (316 mg, 1.28 mmol) in THF (10 mL) STAB (814 mg, 3.84 mmol) was added to the solution. The reaction solution was stirred at room temperature for 2 h. The reaction solution was diluted with water (50 mL), EA (50 mL×3). The organic phases were combined and washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The obtained crude product was subjected to flash column (MeOH/DCM=0～1:4) to obtain 4-(((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)(methyl)amino)methane yl) piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝474.2. LC-MS: (ESI, m/z): [M+H] + = 474.2.
步骤2：4-((甲基(2-(哌啶-4-基)乙基)氨基)甲基)哌啶-1-羧酸苄酯的制备Step 2: Preparation of benzyl 4-((methyl(2-(piperidin-4-yl)ethyl)amino)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000750
Figure PCTCN2022088560-appb-000750
将4-(((2-(1-(叔丁氧羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯(400mg,0.85mmol)的TFA/DCM(10mL,1:4)溶液在室温搅拌1h。反应液直接浓缩得到4-((甲基(2-(哌啶-4-基)乙基)氨基)甲基)哌啶-1-羧酸苄酯。粗产品直接用于下一步反应。Benzyl 4-(((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)(methyl)amino)methyl)piperidine-1-carboxylate (400 mg, 0.85 mmol ) in TFA/DCM (10 mL, 1:4) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain benzyl 4-((methyl(2-(piperidin-4-yl)ethyl)amino)methyl)piperidine-1-carboxylate. The crude product was used directly in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝374.4. LC-MS: (ESI, m/z): [M+H] + = 374.4.
步骤3：4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯的制备Step 3: 4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(tris Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)( Preparation of benzyl methyl)amino)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000751
Figure PCTCN2022088560-appb-000751
向(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.25mmol)的DMF(10mL)溶液中加入4-((甲基(2-(哌啶-4-基)乙基)氨基)甲基)哌啶-1-羧酸苄酯(139mg,0.37mmol)，HATU(142mg,0.37mmol)和DIEA(161mg,1.25mmol)。反应液在室温搅拌2h。反应用水(50mL)淬灭，用EA(50mL×3)萃取。合并有机相并用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，浓缩。所得粗品经层析柱(MeOH:DCM＝0～1:9)纯化得到4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯。 To (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- To a solution of 7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.25 mmol) in DMF (10 mL) was added 4-((methyl(2-( Piperidin-4-yl)ethyl)amino)methyl)piperidine-1-carboxylate benzyl ester (139 mg, 0.37 mmol), HATU (142 mg, 0.37 mmol) and DIEA (161 mg, 1.25 mmol). The reaction solution was stirred at room temperature for 2 h. The reaction was quenched with water (50 mL) and extracted with EA (50 mL x 3). The organic phases were combined and washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The obtained crude product was purified by column chromatography (MeOH:DCM=0～1:9) to obtain 4-(((2-(1-((1R,4R)-4-(4-((((R)-1-() 3-((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane -1-Carbonyl)piperidin-4-yl)ethyl)(methyl)amino)methyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝958.3. LC-MS: (ESI, m/z): [M+H] + = 958.3.
步骤4：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(甲基(哌啶-4-基甲基)氨基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 4: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(methyl(piperidine- 4-ylmethyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl Preparation of esters
Figure PCTCN2022088560-appb-000752
Figure PCTCN2022088560-appb-000752
向4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羧酸苄酯(200mg,0.21mmol)的EtOAc(10mL)溶液中加入Pd(OH) 2/C(60mg,30％)。反应液在70℃下H 2氛围下搅拌4h。反应液过滤，浓缩得到(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(甲基(哌啶-4-基甲基)氨基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。所得产品直接用于下一步反应。 To 4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethane (methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)(methyl) )amino)methyl)piperidine-1-carboxylate benzyl ester (200 mg, 0.21 mmol) in EtOAc (10 mL) was added Pd(OH) 2 /C (60 mg, 30%). The reaction solution was stirred at 70 °C under H 2 atmosphere for 4 h. The reaction solution was filtered and concentrated to obtain (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(methyl( Piperidin-4-ylmethyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxy tert-butyl acid. The obtained product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝824.4. LC-MS: (ESI, m/z): [M+H] + = 824.4.
步骤5：(3-((R)-1-((6-((1R,4R)-4-(4-(2-(((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲基)(甲基)氨基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 5: (3-((R)-1-((6-((1R,4R)-4-(4-(2-(((1-(4-chloro-3-(2,4-di Oxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methyl)(methyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)-7- Preparation of tert-butyl methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000753
Figure PCTCN2022088560-appb-000753
将(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(甲基(哌啶-4-基甲基)氨基)乙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(135mg,0.16mmol)，3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯(69mg,0.16mmol)和DIEA(62mg,0.48mmol)在DMSO(5mL)中的混合液在室温搅拌过夜。反应液倒入水(50mL)中并搅拌10分钟，过滤，滤饼经flash柱(MeOH:DCM＝0～1:4)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(2-(((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲基)(甲基)氨基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。(3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(methyl(piperidine-4- (methyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate 135mg, 0.16mmol), 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester (69mg, 0.16mmol) and DIEA (62mg , 0.48 mmol) in DMSO (5 mL) was stirred at room temperature overnight. The reaction solution was poured into water (50 mL) and stirred for 10 minutes, filtered, and the filter cake was purified by flash column (MeOH:DCM=0～1:4) to obtain (3-((R)-1-((6-(( 1R,4R)-4-(4-(2-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidine Perid-4-yl)methyl)(methyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl yl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1074.2. LC-MS: (ESI, m/z): [M+H] + = 1074.2.
步骤6：1-(5-(4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) (methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl)(methyl) )amino)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000754
Figure PCTCN2022088560-appb-000754
将(3-((R)-1-((6-((1R,4R)-4-(4-(2-(((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)甲基)(甲基)氨基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(120mg,0.11mmol)和TFA/DCM(5mL,1:4)的混合液在室温搅拌1h。反应液直接浓缩，然后用EA(50mL)溶解，用NaHCO 3(aq,30mL×2)。有机相用饱和食盐水(50mL)洗涤，无水Na 2SO 4干燥，过滤，浓缩。粗品经Prep-HPLC纯化得到1-(5-(4-(((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙基)(甲基)氨基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-(2-((((1-(4-chloro-3-(2,4-dioxo) yltetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methyl)(methyl)amino)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy tert-butyl-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (120 mg, 0.11 mmol) and TFA/DCM (5 mL, 1 :4) The mixture was stirred at room temperature for 1 h. The reaction solution was directly concentrated, then dissolved with EA (50 mL) and NaHCO 3 (aq, 30 mL×2). The organic phase was washed with saturated brine (50 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The crude product was purified by Prep-HPLC to give 1-(5-(4-(((2-(1-((1R,4R)-4-(4-((((R)-1-(3-amino-5- (Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl )(methyl)amino)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝974.6. LC-MS: (ESI, m/z): [M+H] + = 974.6.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.18–7.99(m,2H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.8Hz,1H),7.38(d,J＝8.2Hz,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.63–5.47(m,3H),4.49–4.38(m,1H),3.95–3.85(m,4H),3.79-3.69(m,1H),3.67–3.50(m,2H),3.09–2.87(m,3H),2.78-2.63(m,4H),2.35(s,3H),2.33–2.26(m,2H),2.15–2.08(m,4H),1.92–1.48(m,20H),1.40-1.30(m,2H),1.15-0.98(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.49(s,1H),8.18-7.99(m,2H),7.63(d,J=8.2Hz,1H),7.54(d,J=1.8Hz, 1H), 7.38(d, J=8.2Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.63–5.47(m, 3H) ), 4.49–4.38 (m, 1H), 3.95–3.85 (m, 4H), 3.79–3.69 (m, 1H), 3.67–3.50 (m, 2H), 3.09–2.87 (m, 3H), 2.78–2.63 (m, 4H), 2.35 (s, 3H), 2.33–2.26 (m, 2H), 2.15–2.08 (m, 4H), 1.92–1.48 (m, 20H), 1.40–1.30 (m, 2H), 1.15 -0.98(m,4H).
实施例26：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-(2-((3-(1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)丙-2-炔-1-基)氧代)乙基)-N-甲基 环己烷-1-甲酰胺Example 26: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)-N-(2-((3-(1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)) -yl)benzoyl)piperidin-4-yl)prop-2-yn-1-yl)oxo)ethyl)-N-methylcyclohexane-1-carboxamide
步骤1：(3-((R)-1-((6-((1R,4R)-4-((2-羟基乙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 1: (3-((R)-1-((6-((1R,4R)-4-((2-hydroxyethyl)(methyl)carbonyl)cyclohexyl)-7-methoxy- Preparation of tert-butyl 2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000755
Figure PCTCN2022088560-appb-000755
向(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.24mmol)的DMF(5mL)溶液中加入2-(甲氨基)乙烷-1-醇(90mg,1.2mmol)，HATU(137mg,0.36mmol)和DIEA(93mg,0.72mmol)。反应液室温搅拌2h。反应加水(50mL)淬灭，用EA(20mL×3)。有机相用饱和食盐水(60mL)洗涤无水Na 2SO 4干燥，过滤，浓缩。粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-((2-羟基乙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。 To (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- To a solution of 7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.24 mmol) in DMF (5 mL) was added 2-(methylamino)ethane-1 - Alcohol (90 mg, 1.2 mmol), HATU (137 mg, 0.36 mmol) and DIEA (93 mg, 0.72 mmol). The reaction solution was stirred at room temperature for 2h. The reaction was quenched with water (50 mL) and EA (20 mL x 3). The organic phase was washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated. The crude product was purified by flash column (MeOH:DCM=0～1:9) to give (3-((R)-1-((6-((1R,4R)-4-((2-hydroxyethyl)(methyl) (yl)carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝660.2. LC-MS: (ESI, m/z): [M+H] + = 660.2.
步骤2：4-(3-(2-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)乙氧基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯的制备Step 2: 4-(3-(2-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-amido)ethoxy)propan-1 Preparation of -alkyn-1-yl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000756
Figure PCTCN2022088560-appb-000756
将(3-((R)-1-((6-((1R,4R)-4-((2-羟基乙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(150mg,0.22mmol)，4-(3-溴丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(133mg,0.44mmol)和K 2CO 3(151mg,1.1mmol)在乙腈(20mL)中的混合液在70℃搅拌过夜。反应液用水(50mL)稀释，EA(20mL×3)。有机相用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。粗产物经flash柱(MeOH:DCM＝0～1:9)纯化得到4-(3-(2-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)乙氧基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯。 (3-((R)-1-((6-((1R,4R)-4-((2-hydroxyethyl)(methyl)carbonyl)cyclohexyl)-7-methoxy-2- Methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (150 mg, 0.22 mmol), 4-(3-bromoprop-1-yne) A mixture of -1-yl)piperidine-1-carboxylate tert-butyl ester (133 mg, 0.44 mmol) and K2CO3 ( 151 mg , 1.1 mmol) in acetonitrile (20 mL) was stirred at 70 °C overnight. The reaction solution was diluted with water (50 mL), EA (20 mL×3). The organic phase was washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 4-(3-(2-((1R,4R)-4-(4-((((R)-1-(3-( (tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methyl ring Hexane-1-amido)ethoxy)prop-1-yn-1-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝881.3. LC-MS: (ESI, m/z): [M+H] + = 881.3.
步骤3：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基-N-(2-((3-(哌啶-4-基)丙-2-炔-1-基)氧)乙基)环己烷-1-甲酰胺的制备Step 3: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)-N-methyl-N-(2-((3-(piperidin-4-yl)prop-2-yn-1-yl)oxy)ethyl) Preparation of cyclohexane-1-carboxamide
Figure PCTCN2022088560-appb-000757
Figure PCTCN2022088560-appb-000757
向4-(3-(2-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基环己烷-1-酰胺基)乙氧基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(100mg,0.11mmol)的DCM(3mL)溶液中加入TFA(1.0mL)。反应液室温搅拌2h。反应液直接浓缩得到(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基-N-(2-((3-(哌啶-4-基)丙-2-炔-1-基)氧)乙基)环己烷-1-甲酰胺。所得粗产物直接用于下一步反应。To 4-(3-(2-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-methylcyclohexane-1-amido)ethoxy)prop-1-yne To a solution of -1-yl)piperidine-1-carboxylate tert-butyl ester (100 mg, 0.11 mmol) in DCM (3 mL) was added TFA (1.0 mL). The reaction solution was stirred at room temperature for 2h. The reaction solution was directly concentrated to obtain (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy yl-2-methylquinazolin-6-yl)-N-methyl-N-(2-((3-(piperidin-4-yl)prop-2-yn-1-yl)oxy)ethyl base) cyclohexane-1-carboxamide. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝681.3. LC-MS: (ESI, m/z): [M+H] + = 681.3.
步骤4：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-(2-((3-(1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)丙-2-炔-1-基)氧代)乙基)-N-甲基环己烷-1-甲酰胺的制备Step 4: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)-N-(2-((3-(1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)-) Preparation of yl)benzoyl)piperidin-4-yl)prop-2-yn-1-yl)oxo)ethyl)-N-methylcyclohexane-1-carboxamide
Figure PCTCN2022088560-appb-000758
Figure PCTCN2022088560-appb-000758
将(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-甲基-N-(2-((3-(哌啶-4-基)丙-2-炔-1-基)氧)乙基)环己烷-1-甲酰胺(100mg,TFA盐)，4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(60mg,0.14mmol)和DIEA(71mg,0.55mmol)在DMSO(5mL)中的反应液在25℃搅拌过夜。反应液用水(50mL)稀释，过滤。滤液浓缩。所得粗产物经Prep-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％to 95％)纯化得到(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)-N-(2-((3-(1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰基)哌啶-4-基)丙-2-炔-1-基)氧代)乙基)-N-甲基环己烷-1-甲酰胺。 (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)-N-methyl-N-(2-((3-(piperidin-4-yl)prop-2-yn-1-yl)oxy)ethyl)cyclohexyl Alkane-1-carboxamide (100mg, TFA salt), 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester (60mg, 0.14mmol ) and DIEA (71 mg, 0.55 mmol) in DMSO (5 mL) was stirred at 25°C overnight. The reaction solution was diluted with water (50 mL) and filtered. The filtrate was concentrated. The resulting crude product was purified by Prep-HPLC ( CH3CN /0.08% aqueous NH4HCO3 , 5 % to 95%) to give (1R,4R)-4-(4-(((R)-1-(3- Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)-N-(2-((3-(1- (4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)prop-2-yn-1-yl)oxo )ethyl)-N-methylcyclohexane-1-carboxamide.
LC-MS:(ESI,m/z):[M+H] +＝931.4. LC-MS: (ESI, m/z): [M+H] + = 931.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.15(d,J＝7.7Hz,1H),8.07(s,1H),7.62(d,J＝8.2Hz,1H),7.52(d,J＝1.8Hz,1H),7.34(dd,J＝8.2,1.9Hz,1H),6.99(d,J＝5.6Hz,3H),6.76(s,1H),6.45(t,J＝5.9Hz,1H),5.61(d,J＝7.1Hz,1H),4.84-4.61(m,1H),3.95-3.83(m,5H),3.78-3.70(m,1H),3.61-3.51(m,2H),3.50-3.41(m,3H),3.40-3.33(m,2H),3.08(s,1H),3.00-2.90(m,1H),2.83(s,2H),2.78-2.60(m,2H),2.67–2.54(m,3H),2.34(s,3H),1.94-1.78(m,4H),1.74-1.49(m,10H),1.45-1.29(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.15(d, J=7.7Hz, 1H), 8.07(s, 1H), 7.62(d, J=8.2Hz, 1H) ,7.52(d,J＝1.8Hz,1H),7.34(dd,J＝8.2,1.9Hz,1H),6.99(d,J＝5.6Hz,3H),6.76(s,1H),6.45(t, J=5.9Hz, 1H), 5.61(d, J=7.1Hz, 1H), 4.84-4.61(m, 1H), 3.95-3.83(m, 5H), 3.78-3.70(m, 1H), 3.61-3.51 (m,2H),3.50-3.41(m,3H),3.40-3.33(m,2H),3.08(s,1H),3.00-2.90(m,1H),2.83(s,2H),2.78-2.60 (m, 2H), 2.67–2.54 (m, 3H), 2.34 (s, 3H), 1.94-1.78 (m, 4H), 1.74-1.49 (m, 10H), 1.45-1.29 (m, 2H).
实施例27：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 27: 1-(5-(4-(3-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1 -yl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(3-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5- (trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1-yl)piperidine- Preparation of tert-butyl 1-carboxylate
Figure PCTCN2022088560-appb-000759
Figure PCTCN2022088560-appb-000759
将((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(300mg,0.50mmol)，4-(3-溴丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(150mg,0.50mmol)和K 2CO 3(138mg,1.0mmol)在THF(30mL)中的反应液在80℃时搅拌2h。反应液中加水(50mL)，EA(30mL×3)萃取。合并有机相并用饱和食盐水(50mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品flash柱(MeOH:DCM＝0～1:9)纯化得到4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯。 ((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl yl)amino)quinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone (300 mg, 0.50 mmol), 4-(3-bromoprop-1-yn-1-yl)piperidine A reaction of -1-carboxylate tert-butyl ester (150 mg, 0.50 mmol) and K 2 CO 3 (138 mg, 1.0 mmol) in THF (30 mL) was stirred at 80 °C for 2 h. Water (50 mL) was added to the reaction solution, and EA (30 mL×3) was extracted. The organic phases were combined and washed with saturated brine (50 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 4-(3-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(( (R)-1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl ) prop-1-yn-1-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝822.3. LC-MS: (ESI, m/z): [M+H] + = 822.3.
步骤2：4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯的制备Step 2: 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) Amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1-yl)piperidine-1 - Preparation of tert-butyl carboxylate
Figure PCTCN2022088560-appb-000760
Figure PCTCN2022088560-appb-000760
向4-(3-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(170mg,0.2mmol)的EtOH(25mL)溶液中加入Fe(115mg,2.0mmol)和NH 4Cl(106mg,2.0mmol)。反应液在70℃搅拌5h。反应液经硅藻土过滤，滤液浓 缩。所得粗品flash柱(MeOH:DCM＝0～1:9)纯化得到4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯。 To 4-(3-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1-(3-nitro-5-(tri Fluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1-yl)piperidine-1- To a solution of tert-butyl carboxylate (170 mg, 0.2 mmol) in EtOH (25 mL) was added Fe (115 mg, 2.0 mmol) and NH4Cl (106 mg, 2.0 mmol). The reaction solution was stirred at 70°C for 5h. The reaction solution was filtered through celite, and the filtrate was concentrated. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 4-(3-(4-((1R,4R)-4-(4-((((R)-1-(3-amino- 5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl) Prop-1-yn-1-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝792.2. LC-MS: (ESI, m/z): [M+H] + = 792.2.
步骤3：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙-2-炔-1-基)哌嗪-1-基)甲酮的制备Step 3: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)prop-2-yn-1-yl)piperazin-1-yl)methanone preparation
Figure PCTCN2022088560-appb-000761
Figure PCTCN2022088560-appb-000761
向4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羧酸叔丁酯(150mg,0.19mmol)的DCM(3mL)溶液中加入TFA(1.0mL)。反应液在室温搅拌2h。反应液直接浓缩得到((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙-2-炔-1-基)哌嗪-1-基)甲酮。所得粗产物直接用于下一步反应。to 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1-yl)piperidine-1-carboxy To a solution of tert-butyl acid (150 mg, 0.19 mmol) in DCM (3 mL) was added TFA (1.0 mL). The reaction solution was stirred at room temperature for 2 h. The reaction solution was directly concentrated to obtain ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)prop-2-yn-1-yl)piperazin-1-yl)methyl ketone. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝692.2. LC-MS: (ESI, m/z): [M+H] + = 692.2.
步骤4：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1- Preparation of yl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000762
Figure PCTCN2022088560-appb-000762
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙-2-炔-1-基)哌嗪-1-基)甲酮(200mg,0.19mmol)，4-氯-3-(2,4-二基氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(100mg,0.23mmol)和DIEA(73mg,0.57mmol)在DMSO(5mL)中的反应液室温搅拌过夜。反应液中加水(50mL)稀释，DCM(20mL×3)萃取，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品先经flash柱(MeOH:DCM＝0～1:9)纯化，再经Prep-TLC(DCM:MeOH＝10:1)纯化得到1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙-1-炔-1-基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)prop-2-yn-1-yl)piperazin-1-yl)methanone (200mg, 0.19 mmol), pentafluorophenyl 4-chloro-3-(2,4-diyloxotetrahydropyrimidin-1(2H)-yl)benzoate (100 mg, 0.23 mmol) and DIEA (73 mg, 0.57 mmol) ) in DMSO (5 mL) was stirred at room temperature overnight. The reaction solution was diluted with water (50 mL), extracted with DCM (20 mL×3), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was first purified by flash column (MeOH:DCM=0～1:9), and then by Prep-TLC (DCM:MeOH=10:1) to obtain 1-(5-(4-(3-(4-( (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methyl quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)prop-1-yn-1-yl)piperidine-1-carbonyl)-2-chlorophenyl)dihydro Pyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝942.2. LC-MS: (ESI, m/z): [M+H] + = 942.2.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.23-8.10(m,1H),8.06(s,1H),7.61(d,J＝8.2Hz,1H),7.56(d,J＝1.8Hz,1H),7.39(dd,J＝8.2,1.9Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.69–5.39(m,3H),3.88(s,3H),3.78-3.71(m,1H),3.63-3.43(m,6H),3.33-3.20(m,4H),2.94(t,J＝11.2Hz,1H),2.81–2.61(m,4H),2.50-2.40(m,2H),2.40-2.31(m,5H),1.91-1.42(m,16H). 1 H NMR (400MHz, DMSO-d 6 )δ 10.50(s, 1H), 8.23-8.10(m, 1H), 8.06(s, 1H), 7.61(d, J=8.2Hz, 1H), 7.56( d, J=1.8Hz, 1H), 7.39(dd, J=8.2, 1.9Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H) ), 5.69-5.39(m, 3H), 3.88(s, 3H), 3.78-3.71(m, 1H), 3.63-3.43(m, 6H), 3.33-3.20(m, 4H), 2.94(t, J =11.2Hz,1H),2.81-2.61(m,4H),2.50-2.40(m,2H),2.40-2.31(m,5H),1.91-1.42(m,16H).
实施例28：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 28: 1-(5-(4-(3-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propoxy)piperidine- 1-Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯的制备Step 1: Preparation of benzyl 4-(3-(piperazin-1-yl)propoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000763
Figure PCTCN2022088560-appb-000763
向4-(3-((1-((苄氧基)羰基)哌啶-4-基)氧代)丙基)哌嗪-1-羧酸叔丁酯(200mg,0.43mmol)的DCM(3mL)溶液中加入TFA(1mL)，然后室温搅拌2h。反应液直接浓缩得到4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯。所得粗产物直接用于下一步反应。To tert-butyl 4-(3-((1-((benzyloxy)carbonyl)piperidin-4-yl)oxo)propyl)piperazine-1-carboxylate (200 mg, 0.43 mmol) in DCM ( 3 mL) solution was added TFA (1 mL), then stirred at room temperature for 2 h. The reaction solution was directly concentrated to obtain benzyl 4-(3-(piperazin-1-yl)propoxy)piperidine-1-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝362.0. LC-MS: (ESI, m/z): [M+H] + = 362.0.
步骤2：4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯的制备Step 2: 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(tris Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propoxy) Preparation of benzyl piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000764
Figure PCTCN2022088560-appb-000764
边搅拌边向4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯(200mg,TFA盐)的DMF(6mL)溶液中加入(1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.25mmol)，HATU(142mg,0.37mmol)和DIEA(96mg,0.74mmol)。反应液在室温搅拌2h。反应液中加水(60mL)淬灭，EA(20mL×3)萃取。合并有机相并用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(EA:PE＝0～4:1)纯化得到4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯。 To a solution of benzyl 4-(3-(piperazin-1-yl)propoxy)piperidine-1-carboxylate (200 mg, TFA salt) in DMF (6 mL) was added (1R,4R) with stirring -4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy yl-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.25 mmol), HATU (142 mg, 0.37 mmol) and DIEA (96 mg, 0.74 mmol). The reaction solution was stirred at room temperature for 2 h. The reaction solution was quenched by adding water (60 mL), and extracted with EA (20 mL×3). The organic phases were combined and washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～4:1) to obtain 4-(3-(4-((1R,4R)-4-(4-((((R)-1-(3-( (tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperazin-1-yl)propoxy)piperidine-1-carboxylate benzyl.
LC-MS:(ESI,m/z):[M+H] +＝946.1. LC-MS: (ESI, m/z): [M+H] + = 946.1.
步骤3：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 3: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(3-(piperidin-4-yl Preparation of tert-butyl oxy)propyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000765
Figure PCTCN2022088560-appb-000765
搅拌下，向4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羧酸苯甲酯(160mg,0.17mmol)的EA(20mL)溶液中加入Pd(OH) 2/C(80mg)。反应液在70℃下H 2氛围下搅拌过夜。反应液经硅藻土过滤，滤液浓缩得到(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。所得粗产物直接用于下一步反应。 With stirring, add 4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-( Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propoxy ) benzyl piperidine-1-carboxylate (160 mg, 0.17 mmol) in EA (20 mL) was added Pd(OH) 2 /C (80 mg). The reaction solution was stirred at 70 °C under H 2 atmosphere overnight. The reaction solution was filtered through celite, and the filtrate was concentrated to obtain (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4-(3 -(Piperidin-4-yloxy)propyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamic acid tert-butyl ester. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝812.2. LC-MS: (ESI, m/z): [M+H] + = 812.2.
步骤4：(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)丙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 4: (3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)propyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Preparation of tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000766
Figure PCTCN2022088560-appb-000766
将(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(110mg,0.13mmol)，4-氯-3-(2,4-二氧代基-1(2H)-基)苯甲酸五氟苯酯(71mg,0.16mmol)和DIEA(52mg,0.40mmol)在DMSO(3mL)中的反应液在室温搅拌过夜。反应液中加水(50mL)稀释，DCM(20mL×3)萃取。合并有机相并用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗产物经flash柱(MeOH:DCM＝0～1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)丙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4-(3-(piperidin-4-yloxy) propyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (110 mg, 0.13 mmol), Pentafluorophenyl 4-chloro-3-(2,4-dioxo-1(2H)-yl)benzoate (71 mg, 0.16 mmol) and DIEA (52 mg, 0.40 mmol) in DMSO (3 mL) The reaction solution was stirred at room temperature overnight. The reaction solution was diluted with water (50 mL), and extracted with DCM (20 mL×3). The organic phases were combined and washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain (3-((R)-1-((6-((1R,4R)-4-(4-(3-(( 1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)propyl)piperazine-1 -Carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1062.5. LC-MS: (ESI, m/z): [M+H] + = 1062.5.
步骤5：1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propoxy)piperidine-1 Preparation of -carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000767
Figure PCTCN2022088560-appb-000767
向(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)丙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(80mg,0.07mmol)的DCM(3mL)溶液中加入TFA(1.0mL)。反应液在室温搅拌2h。反应液直接浓缩，所得粗品溶解在DCM(20mL)和饱和NaHCO 3(20mL)混合溶液中。所得混合液搅拌30min后，分离有机相，水相用DCM(20mL×2)再萃取。合并有机相并用饱和食盐水(60mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到1-(5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To (3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-chloro-3-(2,4-dioxo) Tetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)propyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinoline To a solution of tert-butyl oxazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (80 mg, 0.07 mmol) in DCM (3 mL) was added TFA (1.0 mL). The reaction solution was stirred at room temperature for 2 h. The reaction solution was directly concentrated, and the obtained crude product was dissolved in a mixed solution of DCM (20 mL) and saturated NaHCO 3 (20 mL). After the resulting mixture was stirred for 30 min, the organic phase was separated, and the aqueous phase was re-extracted with DCM (20 mL×2). The organic phases were combined and washed with saturated brine (60 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 1-(5-(4-(3-(4-((1R,4R)-4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl) Piperazin-1-yl)propoxy)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝962.4. LC-MS: (ESI, m/z): [M+H] + = 962.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.39-8.17(m,1H),8.09(s,1H),7.63(d,J＝8.2Hz,1H),7.57(d,J＝1.8Hz,1H),7.40(dd,J＝8.2,2.0Hz,1H),7.00(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.63–5.49(m,3H),3.95-3.83(m,4H),3.80-3.70(m,1H),3.68-3.57(m,1H),3.57-3.39(m,8H),3.30-3.18(m,2H),3.00-2.90(m,1H),2.79–2.60(m,3H),2.42-2.24(m,9H),1.90-1.77(m,6H),1.72-1.37(m,11H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 8.39-8.17(m, 1H), 8.09(s, 1H), 7.63(d, J=8.2Hz, 1H), 7.57( d, J=1.8Hz, 1H), 7.40(dd, J=8.2, 2.0Hz, 1H), 7.00(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H) ), 5.63-5.49(m, 3H), 3.95-3.83(m, 4H), 3.80-3.70(m, 1H), 3.68-3.57(m, 1H), 3.57-3.39(m, 8H), 3.30-3.18 (m,2H), 3.00-2.90(m,1H), 2.79-2.60(m,3H), 2.42-2.24(m,9H), 1.90-1.77(m,6H), 1.72-1.37(m,11H) .
实施例29：1-(5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 29: 1-(5-(4-(4-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl)piperidine-1 -Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(4-羰基丁基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(4-carbonylbutyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000768
Figure PCTCN2022088560-appb-000768
0℃时向4-(4-羟基丁基)哌啶-1-羧酸叔丁酯(1.2g,4.67mmol)的DCM(20mL)溶液中加入Dess-martin(3.96g,9.34mmol)。反应液室温搅拌过夜。反应液中加入水(50mL)，用DCM(50mL×3)萃取。合并有机相并用饱和食盐水(100mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品先经flash柱(EA:PE＝0～1:4)纯化得到4-(4-羰基丁基)哌啶-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(4-hydroxybutyl)piperidine-1-carboxylate (1.2 g, 4.67 mmol) in DCM (20 mL) was added Dess-martin (3.96 g, 9.34 mmol) at 0 °C. The reaction solution was stirred at room temperature overnight. Water (50 mL) was added to the reaction solution, followed by extraction with DCM (50 mL×3). The organic phases were combined and washed with saturated brine (100 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was first purified by flash column (EA:PE=0～1:4) to obtain tert-butyl 4-(4-carbonylbutyl)piperidine-1-carboxylate.
1H NMR(400MHz,DMSO-d 6)δ9.66(t,J＝1.3Hz,1H),3.91(d,J＝12.0Hz,2H),2.66(s,2H),2.45–2.36(m,2H),1.67–1.48(m,4H),1.43–1.34(m,10H),1.24–1.13(m,2H),0.94(2H). 1 H NMR (400MHz, DMSO-d 6 )δ9.66(t, J=1.3Hz, 1H), 3.91(d, J=12.0Hz, 2H), 2.66(s, 2H), 2.45-2.36(m, 2H), 1.67–1.48 (m, 4H), 1.43–1.34 (m, 10H), 1.24–1.13 (m, 2H), 0.94 (2H).
步骤2：4-(4-(1-(叔-丁氧基羰基)哌啶-4-基)丁基)哌嗪-1-羧酸苯甲酯的制备Step 2: Preparation of benzyl 4-(4-(1-(tert-butoxycarbonyl)piperidin-4-yl)butyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000769
Figure PCTCN2022088560-appb-000769
向4-(4-羰基丁基)哌啶-1-羧酸叔丁酯(390mg,1.53mmol)和哌啶-1-羧酸苯甲酯(390mg,1.53mmol)的THF(10mL)溶液中加入STAB(973mg,4.59mmol)。反应液在室温搅拌2h。反应液中加水(50mL)，EA(50mL×3)萃取。合并有机相并用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(EA:PE＝0～3:2)纯化得到4-(4-(1-(叔-丁氧基羰基)哌啶-4-基)丁基)哌嗪-1-羧酸苯甲酯。 To a solution of tert-butyl 4-(4-carbonylbutyl)piperidine-1-carboxylate (390 mg, 1.53 mmol) and benzyl piperidine-1-carboxylate (390 mg, 1.53 mmol) in THF (10 mL) STAB (973 mg, 4.59 mmol) was added. The reaction solution was stirred at room temperature for 2 h. Water (50 mL) was added to the reaction solution, and EA (50 mL×3) was extracted. The organic phases were combined and washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (EA:PE=0～3:2) to obtain 4-(4-(1-(tert-butoxycarbonyl)piperidin-4-yl)butyl)piperazine-1-carboxylate benzyl acid.
LC-MS:(ESI,m/z):[M+H] +＝460.3. LC-MS: (ESI, m/z): [M+H] + = 460.3.
步骤3：4-(4-(哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(4-(piperazin-1-yl)butyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000770
Figure PCTCN2022088560-appb-000770
搅拌下向4-(4-(1-(叔-丁氧基羰基)哌啶-4-基)丁基)哌嗪-1-羧酸苯甲酯(700mg,1.53mmol)的EtOAc(10mL)溶液中加入Pd(OH) 2/C(210mg,30％)。反应液在70℃时H 2氛围搅拌4h。反应液过滤，滤液浓缩得到4-(4-(哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯。 To benzyl 4-(4-(1-(tert-butoxycarbonyl)piperidin-4-yl)butyl)piperazine-1-carboxylate (700 mg, 1.53 mmol) in EtOAc (10 mL) was added with stirring To the solution was added Pd(OH) 2 /C (210 mg, 30%). The reaction solution was stirred at 70 °C under H 2 atmosphere for 4 h. The reaction solution was filtered, and the filtrate was concentrated to obtain tert-butyl 4-(4-(piperazin-1-yl)butyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝326.2. LC-MS: (ESI, m/z): [M+H] + = 326.2.
步骤4：4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯的制备Step 4: 4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(tris Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl)piperidine Preparation of tert-butyl pyridine-1-carboxylate
Figure PCTCN2022088560-appb-000771
Figure PCTCN2022088560-appb-000771
搅拌下向(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(170mg,0.28mmol)的DMF(10mL)溶液中加入4-(4-(哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(120mg,0.37mmol)，HATU(140mg,0.37mmol)和DIEA(108mg,0.84mmol)。反应液在室温搅拌2h。反应液中加水(50mL)，EA(50mL×3)萃取。合并有机相并用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯. To (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino with stirring )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (170 mg, 0.28 mmol) in DMF (10 mL) was added 4-(4-(piperazine) -1-yl)butyl)piperidine-1-carboxylate tert-butyl ester (120 mg, 0.37 mmol), HATU (140 mg, 0.37 mmol) and DIEA (108 mg, 0.84 mmol). The reaction solution was stirred at room temperature for 2 h. Water (50 mL) was added to the reaction solution, and EA (50 mL×3) was extracted. The organic phases were combined and washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 4-(4-(4-((1R,4R)-4-(4-((((R)-1-(3-() (tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperazin-1-yl)butyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝910.3. LC-MS: (ESI, m/z): [M+H] + = 910.3.
步骤5：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮的制备Step 5: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000772
Figure PCTCN2022088560-appb-000772
将4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(180mg,0.20mmol)的TFA/DCM(5mL,1:4)溶液在室温搅拌1h。反应液直接浓缩得到((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮。4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl)piperidine- A solution of tert-butyl 1-carboxylate (180 mg, 0.20 mmol) in TFA/DCM (5 mL, 1:4) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝710.3. LC-MS: (ESI, m/z): [M+H] + = 710.3.
步骤6：1-(5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl)piperidine-1- Preparation of carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000773
Figure PCTCN2022088560-appb-000773
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮(160mg,0.23mmol))，4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(98mg,0.23mmol)和DIEA(148mg,1.15mmol)在DMSO(5mL)中的反应液室温搅拌过夜。反 应液倒入水(50mL)中，并搅拌10min，过滤，滤饼经Prep-HPLC纯化得到1-(5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazin-1-yl)methanone (160 mg, 0.23 mmol)), 4- Pentafluorophenyl chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (98 mg, 0.23 mmol) and DIEA (148 mg, 1.15 mmol) in DMSO (5 mL) The reaction solution was stirred at room temperature overnight. The reaction solution was poured into water (50 mL), stirred for 10 min, filtered, and the filter cake was purified by Prep-HPLC to obtain 1-(5-(4-(4-(4-((1R,4R)-4-(4- (((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl Alkyl-1-carbonyl)piperazin-1-yl)butyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝960.4. LC-MS: (ESI, m/z): [M+H] + = 960.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.15–7.98(m,2H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.9Hz,1H),7.37(dd,J＝8.2,1.9Hz,1H),6.99(s,1H),6.88(s,1H),6.86(s,1H),6.70(s,1H),5.64–5.48(m,3H),4.50–4.35(m,1H),3.88(s,3H),3.80–3.70(m,1H),3.65–3.55(m,1H),3.51–3.41(m,4H),3.00-2.90(m,2H),2.78-2.61(m,4H),2.38–2.23(m,9H),1.91-1.76(m,4H),1.76–1.37(m,13H),1.35-1.20(m,4H),1.13–1.00(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50 (s, 1H), 8.15-7.98 (m, 2H), 7.63 (d, J=8.2Hz, 1H), 7.54 (d, J=1.9Hz, 1H), 7.37(dd, J=8.2, 1.9Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.64–5.48(m ,3H),4.50-4.35(m,1H),3.88(s,3H),3.80-3.70(m,1H),3.65-3.55(m,1H),3.51-3.41(m,4H),3.00-2.90 (m,2H), 2.78-2.61(m,4H), 2.38-2.23(m,9H), 1.91-1.76(m,4H), 1.76-1.37(m,13H), 1.35-1.20(m,4H) ,1.13–1.00(m,2H).
实施例30：1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 30: 1-(5-(4-(2-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)piperidine- 1-Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-乙氧基-2-羰基乙氧基)哌啶-1-羧酸苯甲酯的制备Step 1: Preparation of benzyl 4-(2-ethoxy-2-carbonylethoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000774
Figure PCTCN2022088560-appb-000774
向4-羟基哌啶-1-羧酸苯甲酯(3.0g,12.7mmol)和NaH(335.0mg,13.9mmol)的THF(30mL)溶液中加入甲基2-溴乙酸酯(3.9g,25.4mmol)，反应液在25℃搅拌过夜。反应用冰水淬灭，EtOAc(30mL×2)。合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经Flash柱(PE:EA＝4:1)纯化得到4-(2-乙氧基-2-羰基乙氧基)哌啶-1-羧酸苯甲酯。 To a solution of benzyl 4-hydroxypiperidine-1-carboxylate (3.0 g, 12.7 mmol) and NaH (335.0 mg, 13.9 mmol) in THF (30 mL) was added methyl 2-bromoacetate (3.9 g, 25.4 mmol), the reaction solution was stirred at 25°C overnight. The reaction was quenched with ice water, EtOAc (30 mL x 2). The organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by Flash column (PE:EA=4:1) to obtain benzyl 4-(2-ethoxy-2-carbonylethoxy)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝308.1. LC-MS: (ESI, m/z): [M+H] + = 308.1.
步骤2：4-(2-羟基乙氧基)哌啶-1-羧酸苯甲酯的制备Step 2: Preparation of benzyl 4-(2-hydroxyethoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000775
Figure PCTCN2022088560-appb-000775
将4-(2-乙氧基-2-羰基乙氧基)哌啶-1-羧酸苯甲酯(1.0g,3.2mmol)和LiBH 4(0.3g,12.8mmol)在THF(15.0mL)中的反应液在60℃搅拌12h。反应用冰水淬灭，然后EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，过滤，减压浓缩得到4-(2-羟基乙氧基)哌啶-1-羧酸苯甲酯。 Benzyl 4-(2-ethoxy-2-carbonylethoxy)piperidine-1-carboxylate (1.0 g, 3.2 mmol) and LiBH4 (0.3 g, 12.8 mmol) in THF (15.0 mL) The reaction solution was stirred at 60 °C for 12 h. The reaction was quenched with ice water, then extracted with EtOAc (30 mL×2), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure to obtain 4-(2-hydroxyethoxy)piperidine Benzyl pyridine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝280.1. LC-MS: (ESI, m/z): [M+H] + = 280.1.
步骤3：4-(2-(甲苯磺酰氧代)乙氧基)哌啶-1-羧酸苯甲酯的制备Step 3: Preparation of benzyl 4-(2-(toluenesulfonyloxo)ethoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000776
Figure PCTCN2022088560-appb-000776
将4-(2-羟基乙氧基)哌啶-1-羧酸苯甲酯(700mg,2.5mmol)，TsCl(570mg,3.0mmol)，TEA(765mg,7.5mmol)和DMAP(24mg,0.2mmol)在DCM(20mL)中的反应液在室温搅拌15h。反应用冰水淬灭，然后EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(PE:EA＝3:1)纯化得到4-(2-(甲苯磺酰氧代)乙氧基)哌啶-1-羧酸苯甲酯。 Benzyl 4-(2-hydroxyethoxy)piperidine-1-carboxylate (700 mg, 2.5 mmol), TsCl (570 mg, 3.0 mmol), TEA (765 mg, 7.5 mmol) and DMAP (24 mg, 0.2 mmol) ) in DCM (20 mL) was stirred at room temperature for 15 h. The reaction was quenched with ice water, then extracted with EtOAc (30 mL×2), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (PE:EA=3:1) to obtain benzyl 4-(2-(toluenesulfonyloxo)ethoxy)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝434.3. LC-MS: (ESI, m/z): [M+H] + = 434.3.
步骤4：4-(2-((1-((苄氧基)羰基)哌啶-4-基)氧代)乙基)哌嗪-1-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 4-(2-((1-((benzyloxy)carbonyl)piperidin-4-yl)oxo)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000777
Figure PCTCN2022088560-appb-000777
将4-(2-(甲苯磺酰氧代)乙氧基)哌啶-1-羧酸苯甲酯(700mg,1.6mmol)，哌嗪-1-羧酸叔丁酯Benzyl 4-(2-(toluenesulfonyloxo)ethoxy)piperidine-1-carboxylate (700 mg, 1.6 mmol), piperazine-1-carboxylate tert-butyl ester
(241mg,1.3mmol)，K 2CO 3(662mg,4.8mmol)和KI(318mg,1.9mmol)在DMF(10mL)中的反应液在70℃搅拌过夜。反应用冰水淬灭，然后EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经层析柱(EtOAc:PE＝0～3:7)纯化得到4-(2-((1-((苄氧基)羰基)哌啶-4-基)氧代)乙基)哌嗪-1-羧酸叔丁酯。 (241 mg, 1.3 mmol), K 2 CO 3 (662 mg, 4.8 mmol) and KI (318 mg, 1.9 mmol) in DMF (10 mL) were stirred at 70° C. overnight. The reaction was quenched with ice water, then extracted with EtOAc (30 mL×2), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by column chromatography (EtOAc:PE=0～3:7) to obtain 4-(2-((1-((benzyloxy)carbonyl)piperidin-4-yl)oxo)ethyl)piperidine tert-butyl oxazine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝448.3. LC-MS: (ESI, m/z): [M+H] + = 448.3.
步骤5：4-(2-(哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯的制备Step 5: Preparation of benzyl 4-(2-(piperazin-1-yl)ethoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000778
Figure PCTCN2022088560-appb-000778
将4-(2-((1-((苄氧基)羰基)哌啶-4-基)氧代)乙基)哌嗪-1-羧酸叔丁酯(390mg,0.87mmol)在TFA/DCM(1mL/3mL)中的反应液在室温搅拌1.0h。反应液直接浓缩得到4-(2-(哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯。4-(2-((1-((benzyloxy)carbonyl)piperidin-4-yl)oxo)ethyl)piperazine-1-carboxylic acid tert-butyl ester (390 mg, 0.87 mmol) in TFA/ The reaction in DCM (1 mL/3 mL) was stirred at room temperature for 1.0 h. The reaction solution was directly concentrated to obtain benzyl 4-(2-(piperazin-1-yl)ethoxy)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝348.2. LC-MS: (ESI, m/z): [M+H] + = 348.2.
步骤6：4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯的制备Step 6: 4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(tris Fluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy) Preparation of benzyl piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000779
Figure PCTCN2022088560-appb-000779
向(1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(85.0mg,0.2mmol)的DMF(2mL)溶液中加入4-(2-(哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯(76.0mg,0.22mmol)，HATU(91.0mg,0.24mmol)和DIEA(59.0mg,0.6mmol)。反应液在室温搅拌2h。.反应用冰水淬灭(20mL)，然后过滤，所得滤饼真空干燥得到4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯。To (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (85.0 mg, 0.2 mmol) in DMF (2 mL) was added 4-(2-(piperidine) Azin-1-yl)ethoxy)piperidine-1-carboxylate benzyl (76.0 mg, 0.22 mmol), HATU (91.0 mg, 0.24 mmol) and DIEA (59.0 mg, 0.6 mmol). The reaction solution was stirred at room temperature for 2 h. The reaction was quenched with ice water (20 mL), then filtered, and the resulting filter cake was dried in vacuo to give 4-(2-(4-((1R,4R)-4-(4-((((R)-1-(3) -((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl Alkyl-1-carbonyl)piperazin-1-yl)ethoxy)piperidine-1-carboxylate benzyl.
LC-MS:(ESI,m/z):[M+H] +＝932.2. LC-MS: (ESI, m/z): [M+H] + = 932.2.
步骤7：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-氧基)乙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 7: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidine-4-oxo) Preparation of tert-butyl) ethyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000780
Figure PCTCN2022088560-appb-000780
将4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羧酸苯甲酯(130.0mg,0.14mmol)和20％Pd(OH) 2/C(60.0mg)的THF(10mL)溶液在60℃下H 2(90psi)氛围搅拌过夜。反应液经硅藻土过滤，滤液减压浓缩得到(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-氧基)乙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)piperidine - Benzyl 1-carboxylate (130.0 mg, 0.14 mmol) and 20% Pd(OH) 2 /C (60.0 mg) in THF (10 mL) was stirred at 60 °C overnight under an atmosphere of H 2 (90 psi). The reaction solution was filtered through celite, and the filtrate was concentrated under reduced pressure to obtain (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4- (2-(Piperidin-4-oxy)ethyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl) tert-butyl carbamate.
LC-MS:(ESI,m/z):[M+H] +＝798.5. LC-MS: (ESI, m/z): [M+H] + = 798.5.
步骤8：(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 8: (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)ethyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Preparation of tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000781
Figure PCTCN2022088560-appb-000781
向(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-氧基)乙基)哌嗪-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(90.0mg,0.14mmol)的DMSO(5mL)溶液中加入DIEA(103.2mg,0.8mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯酸五氟苯酯(73.0mg,0.17mmol)，反应液在室温搅拌2.0h。反应中加水(15mL)淬灭，EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经Prep-HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％～95％)纯化 得到(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 To (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidin-4-oxy)) Ethyl)piperazine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (90.0 mg, 0.14 mmol) DIEA (103.2 mg, 0.8 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester ( 73.0 mg, 0.17 mmol), the reaction solution was stirred at room temperature for 2.0 h. The reaction was quenched by adding water (15 mL), extracted with EtOAc (30 mL×2), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The resulting crude product was purified by Prep-HPLC (acetonitrile/0.05% aqueous NH4HCO3 , 5 %~95%) to give (3-((R)-1-((6-((1R,4R)-4-(4 -(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)ethyl yl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1048.7. LC-MS: (ESI, m/z): [M+H] + = 1048.7.
步骤9：1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 9: 1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)piperidine-1 Preparation of -carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000782
Figure PCTCN2022088560-appb-000782
将(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧代)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(75.0mg,0.1mmol)的TFA/DCM(1.0mL/3.0mL)溶液在室温搅拌1.0h。反应液直接减压浓缩，残余物用8％NaHCO 3水溶液碱化，然后用DCM萃取，分离有机相，用饱和食盐水洗涤，无水Na 2SO 4干燥，减压浓缩得到1-(5-(4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-Chloro-3-(2,4-dioxo) Tetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxo)ethyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinoline A solution of tert-butyl oxazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (75.0 mg, 0.1 mmol) in TFA/DCM (1.0 mL/3.0 mL) at room temperature Stir for 1.0 h. The reaction solution was directly concentrated under reduced pressure, the residue was basified with 8% NaHCO 3 aqueous solution, then extracted with DCM, the organic phase was separated, washed with saturated brine, dried over anhydrous Na 2 SO 4 , and concentrated under reduced pressure to obtain 1-(5- (4-(2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)piperidine-1-carbonyl)-2-chlorobenzene base) dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝948.6. LC-MS: (ESI, m/z): [M+H] + = 948.6.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.13(d,J＝7.5Hz,1H),8.06(s,1H),7.63(d,J＝8.2Hz,2H),7.57(d,J＝1.9Hz,1H),7.40(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.86(d,J＝10.7Hz,2H),6.70(s,1H),5.64–5.46(m,3H),3.95-3.85(m,4H),3.81–3.70(m,1H),3.64–3.53(m,4H),3.53-3.42(m,4H),3.32-3.12(m,2H),2.94(t,J＝11.5Hz,1H),2.80-2.60(m,3H),2.48-2.30(m,7H),1.94-1.74(m,6H),1.72-1.39(m,10H),1.28-1.11(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.13(d, J=7.5Hz, 1H), 8.06(s, 1H), 7.63(d, J=8.2Hz, 2H) ,7.57(d,J＝1.9Hz,1H),7.40(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.86(d,J＝10.7Hz,2H),6.70(s, 1H), 5.64-5.46(m, 3H), 3.95-3.85(m, 4H), 3.81-3.70(m, 1H), 3.64-3.53(m, 4H), 3.53-3.42(m, 4H), 3.32- 3.12(m, 2H), 2.94(t, J=11.5Hz, 1H), 2.80-2.60(m, 3H), 2.48-2.30(m, 7H), 1.94-1.74(m, 6H), 1.72-1.39( m,10H),1.28-1.11(m,2H).
实施例31：1-(5-(9-((4-((1R,4R)-4-((4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 31: 1-(5-(9-((4-((1R,4R)-4-((4-((((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3 -Azaspiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：6,7-二甲氧基-2-甲基喹唑啉-4-醇的制备Step 1: Preparation of 6,7-dimethoxy-2-methylquinazolin-4-ol
Figure PCTCN2022088560-appb-000783
Figure PCTCN2022088560-appb-000783
将2-氨基-4,5-二甲氧基苯甲酸(20.0g，101.5mmol)加入盐酸乙脒(19.1g,203.19mmol)的甲氧基乙醇(120mL)中，140℃搅拌12h，加入H 2O(250mL)搅拌10min，过滤，减压浓缩，得到6,7-二甲氧基-2-甲基喹唑啉-4-醇。 2-Amino-4,5-dimethoxybenzoic acid (20.0 g, 101.5 mmol) was added to acetamidine hydrochloride (19.1 g, 203.19 mmol) in methoxyethanol (120 mL), stirred at 140 °C for 12 h, and H was added 2 O (250 mL) was stirred for 10 min, filtered, and concentrated under reduced pressure to give 6,7-dimethoxy-2-methylquinazolin-4-ol.
LC-MS:(ESI,m/z):[M+H] +＝221.0. LC-MS: (ESI, m/z): [M+H] + = 221.0.
步骤2：7-甲氧基-2-甲基喹唑啉-4,6-二醇的制备Step 2: Preparation of 7-methoxy-2-methylquinazoline-4,6-diol
Figure PCTCN2022088560-appb-000784
Figure PCTCN2022088560-appb-000784
将蛋氨酸(13.16g,92.91mmol)加入到6,7-二甲氧基-2-甲基喹唑啉-4-醇(10.0g,44.4mmol)的甲基磺酸(60mL)中，80℃搅拌过夜，加冰水(20mL)，用NaOH饱和溶液调成中性，在冰水浴下搅拌，过滤，滤饼在乙腈/水(10:1)混合溶液中搅拌，过滤得到7-甲氧基-2-甲基喹唑啉-4,6-二醇。Methionine (13.16 g, 92.91 mmol) was added to 6,7-dimethoxy-2-methylquinazolin-4-ol (10.0 g, 44.4 mmol) in methanesulfonic acid (60 mL), 80°C Stir overnight, add ice water (20 mL), make neutral with saturated NaOH solution, stir under ice water bath, filter, stir the filter cake in acetonitrile/water (10:1) mixed solution, filter to obtain 7-methoxy -2-Methylquinazoline-4,6-diol.
LC-MS:(ESI,m/z):[M+H] +＝207.1. LC-MS: (ESI, m/z): [M+H] + = 207.1.
步骤3：(1R,4R)-4-((4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯的制备Step 3: Preparation of methyl (1R,4R)-4-((4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000785
Figure PCTCN2022088560-appb-000785
将甲基(1S,4S)-4-(甲苯磺酰氧代)环己烷-1-羧酸酯(5.08g,16.1mmol)和K 2CO 3(3.69g,26.8mmol)加入到7-甲氧基-2-甲基喹唑啉-4,6-二醇(2.75g,13.4mmol)的NMP(100mL)溶液中，30℃搅拌过夜，用乙酸乙酯(100mLx3)萃取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品先反相层析(H 2O:ACN＝3:1)纯化，再手性拆分得到(1R,4R)-4-((4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯。 To the 7- Methoxy-2-methylquinazoline-4,6-diol (2.75g, 13.4mmol) in NMP (100mL) solution, stirred at 30°C overnight, extracted with ethyl acetate (100mLx3), saturated brine (150 mL) washed the organic phase, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was first purified by reverse phase chromatography (H 2 O:ACN=3:1), and then chiral resolved to obtain (1R, 4R) -4-((4-Hydroxy-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylate methyl ester.
1H NMR(400MHz,DMSO-d 6)δ12.03(s,1H),7.44(s,1H),7.06(s,1H),4.43–4.33(m,1H),3.87(s,3H),3.61(s,3H),2.44–2.36(m,1H),2.31(s,3H),2.13–2.03(m,2H),1.97(d,J＝13.3Hz,2H),1.57–1.42(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ12.03(s,1H), 7.44(s,1H), 7.06(s,1H), 4.43–4.33(m,1H), 3.87(s,3H), 3.61(s, 3H), 2.44-2.36(m, 1H), 2.31(s, 3H), 2.13-2.03(m, 2H), 1.97(d, J=13.3Hz, 2H), 1.57-1.42(m, 4H).
步骤4：(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯的制备Step 4: (1R,4R)-4-((4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl Preparation of methyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000786
Figure PCTCN2022088560-appb-000786
将BOP(275.9mg,624.2mmol)和DBU(131.8mg,867.1mmol)，(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(137mg,0.45mmol)加入到(1R,4R)-4-((4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯(120mg,346.8mmol)的DMF(100mL)溶液中，70℃搅拌过夜，用乙酸乙酯(100mLx3)萃取，饱和食盐水(150mL)洗涤有机相，无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相层析(H 2O:ACN＝5:1)纯化得到(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯。 BOP (275.9 mg, 624.2 mmol) and DBU (131.8 mg, 867.1 mmol), (R)-(3-(1-aminoethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester (137 mg, 0.45 mmol) was added to (1R,4R)-4-((4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylate methyl acid (120 mg, 346.8 mmol) in DMF (100 mL) solution, stirred at 70 °C overnight, extracted with ethyl acetate (100 mL×3), washed with saturated brine (150 mL), the organic phase, dried over anhydrous sodium sulfate, filtered, and reduced was concentrated under pressure, and the crude product was purified by reverse phase chromatography (H 2 O:ACN=5:1) to give (1R,4R)-4-((4-((((R)-1-(3-((tert-butyl) Oxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1 - Methyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝633.1. LC-MS: (ESI, m/z): [M+H] + = 633.1.
步骤5：(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸的制备Step 5: (1R,4R)-4-((4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylic acid preparation
Figure PCTCN2022088560-appb-000787
Figure PCTCN2022088560-appb-000787
将LiOH(320mg,7619.05mmol)加入到(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸甲酯(300mg,474.7mmol)的THF/H 2O(50ml/25ml)中，50℃搅拌过夜，用柠檬酸溶液(10％)在冰浴下调pH至中性，用乙酸乙酯(200ml)萃取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩得到(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸。 LiOH (320 mg, 7619.05 mmol) was added to (1R,4R)-4-((4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoro Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylate (300 mg, 474.7 mmol) methyl ester THF/H 2 O (50ml/25ml), stirred at 50°C overnight, adjusted the pH to neutrality with citric acid solution (10%) in an ice bath, extracted with ethyl acetate (200ml), washed with saturated brine (150ml) The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give (1R,4R)-4-((4-(((R)-1-(3-((tert-butoxycarbonyl)amino) -5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝619.0. LC-MS: (ESI, m/z): [M+H] + = 619.0.
步骤6：9-((4-((1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苯甲酯的制备Step 6: 9-((4-((1R,4R)-4-((4-((((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoro) Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl)piperazin-1-yl)methyl Preparation of )-3-azaspiro[5.5]undecane-3-carboxybenzyl methyl ester
Figure PCTCN2022088560-appb-000788
Figure PCTCN2022088560-appb-000788
(1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羧酸(280mg,445.86mmol)的DMF(20mL)溶液中，加入9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(280.3mg,728.051mmol)，HATU(276.69mg,728.13mmol)和DIEA(187.8mg,1455.8mmol)，室温搅拌过夜，加水(200mL)并搅拌10min，用乙酸乙酯(100mLx3)萃取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝1:4)纯化得到9-((4-((1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苯甲酯。(1R,4R)-4-((4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carboxylic acid (280 mg, 445.86 mmol) in DMF (20 mL) was added 9-(piperidine) Azin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate benzyl ester (280.3 mg, 728.051 mmol), HATU (276.69 mg, 728.13 mmol) and DIEA (187.8 mg, 1455.8 mmol), stirred overnight at room temperature, added water (200 mL) and stirred for 10 min, extracted with ethyl acetate (100 mL×3), washed the organic phase with saturated brine (150 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. Purified by chromatography (EA:PE=1:4) to give 9-((4-((1R,4R)-4-((4-((((R)-1-(3-((tert-butoxy) Carbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl ) piperazin-1-yl)methyl)-3-azaspiro[5.5]undecane-3-carboxylate benzyl.
LC-MS:(ESI,m/z):[M+H] +＝986.1. LC-MS: (ESI, m/z): [M+H] + = 986.1.
步骤7：(3-((R)-1-((6-(((1R,4R)-4-(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 7: (3-((R)-1-((6-(((1R,4R)-4-(4-((3-azaspiro[5.5]undecan-9-yl)methyl) )piperazine-1-carbonyl)cyclohexyl)oxo)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl) Preparation of tert-butyl carbamate
Figure PCTCN2022088560-appb-000789
Figure PCTCN2022088560-appb-000789
将9-((4-((1R,4R)-4-((4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苯甲酯(360mg,0.582mmol)溶解在乙酸乙酯(20mL)中，加入Pd(OH) 2(72mg,20％)，50℃搅拌2h，过滤，浓缩干燥得到(3-((R)-1-((6-(((1R,4R)-4-(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 9-((4-((1R,4R)-4-((4-((((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)- Benzyl 3-azaspiro[5.5]undecane-3-carboxylate (360 mg, 0.582 mmol) was dissolved in ethyl acetate (20 mL), added Pd(OH) 2 (72 mg, 20%), 50°C Stir for 2 h, filter, concentrate and dry to obtain (3-((R)-1-(((6-(((1R,4R)-4-(4-((3-azaspiro[5.5]undecane-9 -yl)methyl)piperazine-1-carbonyl)cyclohexyl)oxo)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl) group) phenyl) tert-butyl carbamate.
LC-MS-MC21-1867-57:[M+H] +＝852.2. LC-MS-MC21-1867-57: [M+H] + = 852.2.
步骤8：(3-((R)-1-((6-(((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二羰基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 8: (3-((R)-1-((6-(((1R,4R)-4-(4-((3-(4-chloro-3-(2,4-dicarbonyltetrahydro) Pyrimidine-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)oxo)-7-methyl Preparation of tert-butyl oxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000790
Figure PCTCN2022088560-appb-000790
(3-((R)-1-((6-(((1R,4R)-4-(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(230mg,0.272mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯酸五氟苯酯(140.7mg,0.324mmol)用DMSO(5mL)溶解，DIEA(100mg,0.775mmol)加入，然后反应液室温搅拌2小时，水(50mL)加入到反应液中，搅拌2分钟，过滤，得到粗产品(3-((R)-1-((6-(((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二羰基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。(3-((R)-1-((6-(((1R,4R)-4-(4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine -1-Carbonyl)cyclohexyl)oxo)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamic acid tert. Butyl ester (230 mg, 0.272 mmol) and pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (140.7 mg, 0.324 mmol) in DMSO (5mL) was dissolved, DIEA (100mg, 0.775mmol) was added, then the reaction solution was stirred at room temperature for 2 hours, water (50mL) was added to the reaction solution, stirred for 2 minutes, and filtered to obtain the crude product (3-((R)-1 -((6-(((1R,4R)-4-(4-((3-(4-chloro-3-(2,4-dicarbonyltetrahydropyrimidin-1(2H)-yl)benzoyl) )-3-Azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)oxo)-7-methoxy-2-methylquinazoline-4 -yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1102.0. LC-MS: (ESI, m/z): [M+H] + = 1102.0.
步骤9：1-(5-(9-((4-((1R,4R)-4-((4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 9: 1-(5-(9-((4-((1R,4R)-4-((4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3- Preparation of azaspiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000791
Figure PCTCN2022088560-appb-000791
(3-((R)-1-((6-(((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二羰基四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)氧代)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(250mg,0.227mmol)用二氯甲烷(20mL)溶解，三氟乙酸(5ml)加入，然后反应液室温搅拌2小时，加入饱和碳酸氢钠水溶液,调节pH至中性，用乙酸乙酯萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，所得粗品经反相制备纯化得到1-(5-(9-((4-((1R,4R)-4-((4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)氧代)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((R)-1-((6-(((1R,4R)-4-(4-((3-(4-Chloro-3-(2,4-dicarbonyltetrahydropyrimidine-1 (2H)-yl)benzoyl)-3-azaspiro[5.5]undec-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)oxo)-7-methoxy- 2-Methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamic acid tert-butyl ester (250 mg, 0.227 mmol) was dissolved in dichloromethane (20 mL), three Fluoroacetic acid (5ml) was added, then the reaction solution was stirred at room temperature for 2 hours, saturated aqueous sodium bicarbonate solution was added, pH was adjusted to neutral, extracted with ethyl acetate, the organic phase was washed with saturated brine (100mL), and dried over anhydrous sodium sulfate , filtered, concentrated under reduced pressure, and the obtained crude product was purified by reverse-phase preparation to obtain 1-(5-(9-((4-((1R,4R)-4-((4-((((R)-1-(3 -Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)oxo)cyclohexane-1-carbonyl)piperidine Azin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1002.1. LC-MS: (ESI, m/z): [M+H] + = 1002.1.
1H NMR(400MHz,MeOD)δ8.45(s,1H),7.88(s,1H),7.66(d,J＝8.2Hz,1H),7.56(s,1H),7.44(d,J＝8.1Hz,1H),7.07(s,1H),6.98(s,2H),6.84(s,1H),5.75(q,J＝6.8Hz,1H),4.57-4.47(m,1H),4.00(s,3H),3.84-3.61(m,8H),3.51-3.49(m,2H),2.93-2.72(m,3H),2.61-2.42(m,7H),2.34-2.21(m,4H),1.95-1.33(m,18H),1.30-1.03(m,4H). 1 H NMR (400MHz, MeOD) δ8.45(s, 1H), 7.88(s, 1H), 7.66(d, J=8.2Hz, 1H), 7.56(s, 1H), 7.44(d, J=8.1 Hz, 1H), 7.07(s, 1H), 6.98(s, 2H), 6.84(s, 1H), 5.75(q, J=6.8Hz, 1H), 4.57-4.47(m, 1H), 4.00(s ,3H),3.84-3.61(m,8H),3.51-3.49(m,2H),2.93-2.72(m,3H),2.61-2.42(m,7H),2.34-2.21(m,4H),1.95 -1.33(m,18H),1.30-1.03(m,4H).
实施例32：1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 32: 1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine -1-Carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000792
Figure PCTCN2022088560-appb-000792
将4-((2-(1-(叔-丁氧基羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苯甲酯(300.0mg,0.6mmol)和10％Pd(OH) 2/C(150.0mg)在THF(20mL)中的混合液在70℃下H 2(60psi)氛围中搅拌12h。反应液过滤，滤液减压浓缩得到4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯。 Benzyl 4-((2-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate (300.0 mg, 0.6 mmol) and A mixture of 10% Pd(OH) 2 /C (150.0 mg) in THF (20 mL) was stirred at 70 °C under an atmosphere of H 2 (60 psi) for 12 h. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure to obtain tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝325.3. LC-MS: (ESI, m/z): [M+H] + = 325.3.
步骤2：4-(2-((1-(3-(2,4-二羰基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 2: 4-(2-((1-(3-(2,4-Dicarbonyltetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoyl)piperidin-4-yl) Preparation of tert-butyl methoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000793
Figure PCTCN2022088560-appb-000793
向4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(170mg,0.52mmol)的DMSO(5mL)溶液中加入DIEA(103.2mg,0.8mmol)和3-(2,4-二羰基四氢嘧啶-1(2H)-基)-4-甲氧基苯酸五氟苯酯(247mg,0.57mmol)，反应液在室温搅拌2h。反应用水淬灭，然后用EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，无水Na 2SO 4干燥，浓缩。所得粗品经Flash(PE:EA＝3:1)纯化得到4-(2-((1-(3-(2,4-二羰基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate (170 mg, 0.52 mmol) in DMSO (5 mL) was added DIEA (103.2 mg, 0.8 mmol) and 3-(2,4-dicarbonyltetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester (247 mg, 0.57 mmol), the reaction solution was stirred at room temperature for 2 h. The reaction was quenched with water, then extracted with EtOAc (30 mL×2), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 and concentrated. The resulting crude product was purified by Flash (PE:EA=3:1) to give 4-(2-((1-(3-(2,4-dicarbonyltetrahydropyrimidin-1(2H)-yl)-4-methoxy benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝573.2. LC-MS: (ESI, m/z): [M+H] + = 573.2.
步骤3：1-(2-甲氧基-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Methoxy-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine- Preparation of 2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000794
Figure PCTCN2022088560-appb-000794
将4-(2-((1-(3-(2,4-二羰基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔 丁酯(200mg,0.42mmol)的TFA/DCM(1mL/3mL)溶液在室温搅拌1h。反应液直接浓缩得到1-(2-甲氧基-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。所得粗产物直接用于下一步反应。4-(2-((1-(3-(2,4-Dicarbonyltetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoyl)piperidin-4-yl)methoxy (200 mg, 0.42 mmol) in TFA/DCM (1 mL/3 mL) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain 1-(2-methoxy-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydro Pyrimidine-2,4(1H,3H)-dione. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝473.1. LC-MS: (ESI, m/z): [M+H] + = 473.1.
步骤4：4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 4: 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Preparation of methyl methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000795
Figure PCTCN2022088560-appb-000795
向4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(200mg,0.61mmol)，DBU(228mg,1.5mmol)和BOP(404mg,0.91mmol)的DMF(5mL)混合液中加入(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(273mg,0.91mmol)。反应液在70℃搅拌14h。反应液中加水，然后用EtOAc(30mL×2)萃取，合并有机相并用饱和食盐水洗涤，经无水Na 2SO 4干燥。有机相减压浓缩，所得粗品经Flash柱(PE:EA＝1:1)纯化得到4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 To methyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate (200 mg, 0.61 mmol), DBU (228 mg, To a mixture of 1.5 mmol) and BOP (404 mg, 0.91 mmol) in DMF (5 mL) was added tert-butyl (R)-(3-(1-aminoethyl)-5-(trifluoromethyl)phenyl)carbamate ester (273 mg, 0.91 mmol). The reaction solution was stirred at 70°C for 14h. Water was added to the reaction solution, followed by extraction with EtOAc (30 mL×2). The organic phases were combined, washed with saturated brine, and dried over anhydrous Na 2 SO 4 . The organic phase was concentrated under reduced pressure, and the obtained crude product was purified by Flash column (PE:EA=1:1) to obtain 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)- 5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝615.3. LC-MS: (ESI, m/z): [M+H] + = 615.3.
步骤5：4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸的制备Step 5: 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Preparation of yl-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid
Figure PCTCN2022088560-appb-000796
Figure PCTCN2022088560-appb-000796
将4-(4-(((R)-1-(3-((叔-丁氧基羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(150mg,0.24mmol)和LiOH(110mg,4.8mmol)在THF/H 2O(4mL/2mL)中的混合液在50℃搅拌15h。反应液减压浓缩得到4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸。 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Methyl-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate (150 mg, 0.24 mmol) and LiOH (110 mg, 4.8 mmol) in THF/H 2 O (4 mL/ The mixture in 2 mL) was stirred at 50 °C for 15 h. The reaction solution was concentrated under reduced pressure to obtain 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝601.2. LC-MS: (ESI, m/z): [M+H] + = 601.2.
步骤6：(3-((1R)-1-((6-(4-(4-(2-((1-(3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 6: (3-((1R)-1-((6-(4-(4-(2-((1-(3-(2,4-dioxotetrahydropyrimidine-1(2H)) -yl)-4-methoxybenzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy Preparation of tert-butyl-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000797
Figure PCTCN2022088560-appb-000797
将4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸(120.0mg,0.2mmol)，1-(2-甲氧基-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(104mg,0.22mmol)，HATU(91.0mg,0.24mmol)和DIEA(59.0mg,0.6mmol)在DMF(3mL)中的混合液在室温搅拌2h。反应液中加水，过滤，滤饼经Prep-HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％～95％)纯化得到(3-((1R)-1-((6-(4-(4-(2-((1-(3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨 基甲酸叔丁酯。 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid (120.0 mg, 0.2 mmol), 1-(2-methoxy-5-(4-((2-( Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (104 mg, 0.22 mmol), HATU (91.0 mg) , 0.24 mmol) and DIEA (59.0 mg, 0.6 mmol) in DMF (3 mL) was stirred at room temperature for 2 h. Water was added to the reaction solution, filtered, and the filter cake was purified by Prep-HPLC (acetonitrile/0.05% NH 4 HCO 3 aqueous solution, 5%～95%) to obtain (3-((1R)-1-((6-(4-( 4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoyl)piperidin-4-yl)methan oxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5 -(trifluoromethyl)phenyl)carbamate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1056.6. LC-MS: (ESI, m/z): [M+H] + = 1056.6.
步骤7：1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine- Preparation of 1-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000798
Figure PCTCN2022088560-appb-000798
将(3-((1R)-1-((6-(4-(4-(2-((1-(3-(2,4-二氧代基四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(100.0mg,0.1mmol)在TFA/DCM(1mL/3mL)中的反应液在室温搅拌1h。反应液浓缩，残余物用8％NaHCO 3水溶液碱化，然后用DCM(20mL×3)萃取，有机相用饱和食盐水洗涤，无水硫酸钠干燥，减压浓缩得到1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((1R)-1-((6-(4-(4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) )-4-Methoxybenzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy- 2-Methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (100.0 mg, 0.1 mmol) in TFA/DCM (1 mL/3 mL) The reaction solution was stirred at room temperature for 1 h. The reaction solution was concentrated, the residue was basified with 8% NaHCO 3 aqueous solution, then extracted with DCM (20 mL×3), the organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 1-(5-(4 -((2-(1-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-methoxybenzene base) dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝955.2. LC-MS: (ESI, m/z): [M+H] + = 955.2.
1H NMR(400MHz,DMSO-d 6)δ10.33(s,1H),8.29(s,1H),8.08(s,1H),7.38(dd,J＝8.5,2.1Hz,1H),7.32(d,J＝2.0Hz,1H),7.15(d,J＝8.6Hz,1H),6.99(s,1H),6.89(s,1H),6.85(s,1H),6.69(s,1H),5.83(s,1H),5.60-5.50(m,3H),4.47-4.33(m,1H),4.00-3.90(m,1H),3.86(s,3H),3.84(s,3H),3.61-3.58(t,J＝6.7Hz,2H),3.45-3.38(t,J＝6.3Hz,2H),3.33-3.28(m,2H),3.25-3.21(d,J＝6.3Hz,2H),3.08-2.97(m,1H),2.95-2.82(m,2H),2.70-2.65(t,J＝6.4Hz,2H),2.58-2.52(m,2H),2.40-2.32(m,5H),2.25-2.15(m,1H),1.90-1.38(m,13H),1.28-0.92(m,5H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.33 (s, 1H), 8.29 (s, 1H), 8.08 (s, 1H), 7.38 (dd, J=8.5, 2.1 Hz, 1H), 7.32 ( d, J=2.0Hz, 1H), 7.15(d, J=8.6Hz, 1H), 6.99(s, 1H), 6.89(s, 1H), 6.85(s, 1H), 6.69(s, 1H), 5.83(s,1H),5.60-5.50(m,3H),4.47-4.33(m,1H),4.00-3.90(m,1H),3.86(s,3H),3.84(s,3H),3.61- 3.58(t,J＝6.7Hz,2H),3.45-3.38(t,J＝6.3Hz,2H),3.33-3.28(m,2H),3.25-3.21(d,J＝6.3Hz,2H),3.08 -2.97(m, 1H), 2.95-2.82(m, 2H), 2.70-2.65(t, J=6.4Hz, 2H), 2.58-2.52(m, 2H), 2.40-2.32(m, 5H), 2.25 -2.15(m,1H),1.90-1.38(m,13H),1.28-0.92(m,5H).
实施例33：1-(5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 33: 1-(5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)methyl )piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-羟基乙基)哌嗪-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000799
Figure PCTCN2022088560-appb-000799
将哌嗪-1-羧酸叔丁酯(1.0g,5.38mmol)，2-溴乙烷-1-醇(0.67g,5.38mmol)和K 2CO 3(1.48g,10.76mmol)在DMF(20mL)中的反应液室温搅拌过夜。向反应液中加水(50mL)，然后用EA(50mL×3)萃取。有机相用饱和食盐水(100mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到4-(2-羟基乙基)哌嗪-1-羧酸叔丁酯。 Combine piperazine-1-carboxylate tert-butyl ester (1.0 g, 5.38 mmol), 2-bromoethane-1-ol (0.67 g, 5.38 mmol) and K 2 CO 3 (1.48 g, 10.76 mmol) in DMF ( The reaction solution in 20 mL) was stirred at room temperature overnight. Water (50 mL) was added to the reaction solution, followed by extraction with EA (50 mL×3). The organic phase was washed with saturated brine (100 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain tert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylate.
1H NMR(400MHz,MeOD)δ3.67(t,J＝5.9Hz,2H),3.47–3.39(m,4H),2.53(t,J＝5.9Hz,2H),2.50–2.42(m,4H),1.45(s,9H). 1 H NMR(400MHz,MeOD)δ3.67(t,J=5.9Hz,2H),3.47-3.39(m,4H),2.53(t,J=5.9Hz,2H),2.50-2.42(m,4H) ),1.45(s,9H).
步骤2：4-(2-(吡啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(2-(pyridin-4-ylmethoxy)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000800
Figure PCTCN2022088560-appb-000800
0℃向4-(2-羟基乙基)哌嗪-1-羧酸叔丁酯(400mg,1.74mmol)的无水THF(10mL)溶液中加入NaH(140mg,60％,3.48mmol)并搅拌2h。然后加入4-(溴甲基)吡啶氢溴化(528mg,2.09mmol)，然后反应液室温搅拌过夜。反应液中加水(50mL)，然后用EA(50mL×3)萃取。有机相用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经层析柱(MeOH:DCM＝0～1:9)纯化得到4-(2-(吡啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(2-hydroxyethyl)piperazine-1-carboxylate (400 mg, 1.74 mmol) in dry THF (10 mL) at 0°C was added NaH (140 mg, 60%, 3.48 mmol) and stirred 2h. Then 4-(bromomethyl)pyridine hydrobromide (528 mg, 2.09 mmol) was added and the reaction was stirred at room temperature overnight. Water (50 mL) was added to the reaction solution, followed by extraction with EA (50 mL×3). The organic phase was washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by column chromatography (MeOH:DCM=0˜1:9) to obtain tert-butyl 4-(2-(pyridin-4-ylmethoxy)ethyl)piperazine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝322.6. LC-MS: (ESI, m/z): [M+H] + = 322.6.
步骤3：4-(2-(哌啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000801
Figure PCTCN2022088560-appb-000801
搅拌下向4-(2-(吡啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯(600mg,2.60mmol)的i-PrOH/H 2O(13mL,6:7)溶液中加入Pd/C(180mg)。然后反应液在75℃下H 2氛围搅拌过夜。反应液过滤，减压浓缩得到4-(2-(哌啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯。所得粗产物直接用于下一步反应。 To a stirred solution of tert-butyl 4-(2-(pyridin-4-ylmethoxy)ethyl)piperazine-1-carboxylate (600 mg, 2.60 mmol) in i-PrOH/H 2 O (13 mL, 6: 7) Pd/C (180 mg) was added to the solution. The reaction was then stirred overnight at 75 °C under a H2 atmosphere. The reaction solution was filtered and concentrated under reduced pressure to obtain tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperazine-1-carboxylate. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝328.2. LC-MS: (ESI, m/z): [M+H] + = 328.2.
步骤4：4-(2-((1-(4-氯-3-(2,4-二羰基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯的制备Step 4: 4-(2-((1-(4-Chloro-3-(2,4-dicarbonyltetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy Preparation of tert-butyl)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000802
Figure PCTCN2022088560-appb-000802
向4-(2-(哌啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯(180mg,0.55mmol)的DMSO(5mL)溶液中加入DIEA(213mg,1.65mmol)和4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯酸五氟苯酯(238mg,0.55mmol)。反应液在室温搅拌2h。反应液中加水(50mL)，然后用EA(50mL×3)萃取。有机相用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到4-(2-((1-(4-氯-3-(2,4-二羰基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯。 To a solution of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperazine-1-carboxylate (180 mg, 0.55 mmol) in DMSO (5 mL) was added DIEA (213 mg, 1.65 mmol) ) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester (238 mg, 0.55 mmol). The reaction solution was stirred at room temperature for 2 h. Water (50 mL) was added to the reaction solution, followed by extraction with EA (50 mL×3). The organic phase was washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain 4-(2-((1-(4-chloro-3-(2,4-dicarbonyltetrahydropyrimidine-1(2H)- yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝578.2. LC-MS: (ESI, m/z): [M+H] + = 578.2.
步骤5：1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(2-Chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2, Preparation of 4(1H,3H)-dione
Figure PCTCN2022088560-appb-000803
Figure PCTCN2022088560-appb-000803
将4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯(160mg,0.28mmol)在TFA/DCM(5mL,1:4)中的溶液室温搅拌1h。反应液直接浓缩得到1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。所得粗产物直接用于下一步反应。4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy (yl)ethyl)piperazine-1-carboxylate tert-butyl ester (160 mg, 0.28 mmol) in TFA/DCM (5 mL, 1:4) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain 1-(2-chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine- 2,4(1H,3H)-dione. The obtained crude product was directly used in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝478.3. LC-MS: (ESI, m/z): [M+H] + = 478.3.
步骤6：(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯的制备Step 6: (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-Chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2- Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate
Figure PCTCN2022088560-appb-000804
Figure PCTCN2022088560-appb-000804
将1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(160mg)，(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.25mmol)，HATU(143mg,0.38mmol)和DIEA(160mg,1.25mmol)在DMF(5mL)溶液中的混合物室温搅拌过夜。反应液中加入水(50mL)，然后用EA(50mL×3)萃取。有机相用饱和食盐水(150mL)洗涤，无水Na 2SO 4干燥，过滤，减压浓缩。所得粗品经flash柱(MeOH:DCM＝0～1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪 -1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯。 1-(2-Chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione (160 mg), (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.25 mmol), HATU (143 mg, 0.38 mmol) A mixture of DIEA (160 mg, 1.25 mmol) in DMF (5 mL) was stirred at room temperature overnight. Water (50 mL) was added to the reaction solution, followed by extraction with EA (50 mL×3). The organic phase was washed with saturated brine (150 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The obtained crude product was purified by flash column (MeOH:DCM=0～1:9) to obtain (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1 -(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1 -Carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1062.1. LC-MS: (ESI, m/z): [M+H] + = 1062.1.
步骤7：1-(5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(5-(4-((2-(4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)methyl) Preparation of piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000805
Figure PCTCN2022088560-appb-000805
将(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-氯-3-(2,4-二氧代基四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)氨基甲酸叔丁酯(100mg,0.09mmol)的TFA/DCM(5mL,1:4)溶液在室温搅拌1h。反应液直接浓缩，粗品经Prep-HPLC纯化得到1-(5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(4-Chloro-3-(2,4-dioxo) Tetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carbamate (100 mg, 0.09 mmol) in TFA/DCM (5 mL, 1:4) at room temperature Stir for 1 h. The reaction solution was directly concentrated, and the crude product was purified by Prep-HPLC to obtain 1-(5-(4-((2-(4-((1R,4R)-4-(4-((((R)-1-(3- Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1- yl)ethoxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝962.4. LC-MS: (ESI, m/z): [M+H] + = 962.4.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.20-8.10(m,1H),8.05(s,1H),7.62(d,J＝8.2Hz,1H),7.54(s,1H),7.37(d,J＝8.1Hz,1H),6.99(s,1H),6.86(d,J＝10.0Hz,2H),6.70(s,1H),5.63–5.44(m,3H),4.51–4.38(m,1H),3.89(s,3H),3.80–3.70(m,1H),3.68-3.52(m,2H),3.53-3.40(m,6H),3.27-3.24(m,2H),3.04-2.94(m,2H),2.81-2.61(m,5H),2.45-2.30(m,7H),1.92-1.45(m,15H),1.20-1.01(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.49(s, 1H), 8.20-8.10(m, 1H), 8.05(s, 1H), 7.62(d, J=8.2Hz, 1H), 7.54( s, 1H), 7.37(d, J=8.1Hz, 1H), 6.99(s, 1H), 6.86(d, J=10.0Hz, 2H), 6.70(s, 1H), 5.63–5.44(m, 3H) ), 4.51–4.38(m, 1H), 3.89(s, 3H), 3.80–3.70(m, 1H), 3.68-3.52(m, 2H), 3.53-3.40(m, 6H), 3.27-3.24(m ,2H),3.04-2.94(m,2H),2.81-2.61(m,5H),2.45-2.30(m,7H),1.92-1.45(m,15H),1.20-1.01(m,2H).
实施例34：1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 34: 1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-nitrogen Heterospiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(R)-4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯的制备Step 1: (R)-4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methyl Preparation of tert-butyl quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000806
Figure PCTCN2022088560-appb-000806
将(R)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(220mg,0.44mmol)用乙酸乙酯(12mL)溶解并冷却到0℃，N-Boc哌嗪(163mg,0.88mmol)，DIEA(169mg,1.31mmol)和T 3P(209mg,0.66mmol)分别加入，反应液在0℃搅拌3小时，用水(30mL)淬灭，乙酸乙酯(30mL×3)萃取，有机相用饱和食盐水(20mL)洗一次，无水硫酸钠干燥，过滤并减压浓缩，粗产品经柱层析(PE:EA＝10:1)纯化得到(R)-4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯。 (R)-4-(4-((1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexane-1-carboxylic acid (220 mg, 0.44 mmol) was dissolved in ethyl acetate (12 mL) and cooled to 0°C, N-Boc piperazine (163 mg, 0.88 mmol), DIEA (169 mg, 1.31 mmol) ) and T 3 P (209 mg, 0.66 mmol) were added respectively, the reaction solution was stirred at 0° C. for 3 hours, quenched with water (30 mL), extracted with ethyl acetate (30 mL×3), and the organic phase was washed with saturated brine (20 mL). Once, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure, the crude product was purified by column chromatography (PE:EA=10:1) to obtain (R)-4-(4-(4-((1-(3- Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1- tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝671.3. LC-MS: (ESI, m/z): [M+H] + = 671.3.
步骤2：(R)-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮的制备Step 2: (R)-(4-(4-((1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinoline Preparation of oxazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone
Figure PCTCN2022088560-appb-000807
Figure PCTCN2022088560-appb-000807
将(R)-4-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-羧酸叔丁酯(220mg,0.33mmol)加入到氯化氢的乙酸乙酯溶液中(3M/EA,10mL)，反应液室温搅拌2小时，直接减压浓缩得到(R)-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮，无需纯化直接用于下一步。(R)-4-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1-carboxylate tert-butyl ester (220mg, 0.33mmol) was added to a solution of hydrogen chloride in ethyl acetate (3M/EA, 10mL), the reaction solution Stir at room temperature for 2 hours, and directly concentrate under reduced pressure to obtain (R)-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy yl-2-methylquinazolin-6-yl)cyclohexyl)(piperazin-1-yl)methanone was used in the next step without purification.
步骤3：1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-aza Preparation of spiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000808
Figure PCTCN2022088560-appb-000808
将(R)-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(哌嗪-1-基)甲酮(115mg,0.165mmol)用四氢呋喃(5mL)溶解，2-(3-(4-氯-3-(2,4-氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙醛(39mg,0.09mmol)和三乙酰氧基硼氢化钠(55mg,0.27mmol)依次加入，反应液室温搅拌2小时，用水(10mL)淬灭，二氯甲烷(30mL×3)萃取，无水硫酸钠干燥，过滤并减压浓缩，粗产品使用反相制备(先甲酸体系纯化，后用碳酸氢铵体系纯化)得到1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(R)-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline -6-yl)cyclohexyl)(piperazin-1-yl)methanone (115 mg, 0.165 mmol) was dissolved in tetrahydrofuran (5 mL), 2-(3-(4-chloro-3-(2,4-oxo) Tetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)acetaldehyde (39 mg, 0.09 mmol) and sodium triacetoxyborohydride (55 mg) , 0.27 mmol) were added sequentially, the reaction solution was stirred at room temperature for 2 hours, quenched with water (10 mL), extracted with dichloromethane (30 mL × 3), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure, the crude product was prepared using reversed phase ( Purification with formic acid system first, then purification with ammonium bicarbonate system) to obtain 1-(5-(9-(2-(4-((1S,4S)-4-(4-(((R)-1-(3 -Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1 -yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1000.1. LC-MS: (ESI, m/z): [M+H] + = 1000.1.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.31(d,J＝7.9Hz,1H),7.95(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.9Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),6.98(s,1H),6.88(s,1H),6.84(s,1H),6.69(s,1H),5.66–5.42(m,3H),3.87(s,3H),3.75-3.50(m,5H),3.50-3.40(m,5H),3.00-2.70(m,5H),2.39-2.23(m,7H),2.00-1.84(m,4H),1.75-1.63(m,6H),1.59-1.18(m,13H),1.13-0.96(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.31(d, J=7.9Hz, 1H), 7.95(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝1.9Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),6.98(s,1H),6.88(s,1H),6.84(s,1H),6.69( s,1H),5.66-5.42(m,3H),3.87(s,3H),3.75-3.50(m,5H),3.50-3.40(m,5H),3.00-2.70(m,5H),2.39- 2.23(m,7H),2.00-1.84(m,4H),1.75-1.63(m,6H),1.59-1.18(m,13H),1.13-0.96(m,4H).
实施例35：1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(乙氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 35: 1-(2-Chloro-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(ethylamino)-5- (Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl )-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000809
Figure PCTCN2022088560-appb-000809
向1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮(70mg,0.071mmol)的THF(3ml)溶液中加入乙醛(40％水溶液,16mg,0.142mmol)，混合液在室温搅拌30分钟后，加入三乙酰氧基硼氢化钠(75mg,0.355mmol)并室温搅拌过夜。反应液用水(15mL)稀释，DCM(20×3ml)萃取，无水Na 2SO 4干燥，过滤并减压浓缩，所得粗品经prep-HPLC纯化得到1-(2-氯-5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-(乙氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 To 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5] To a solution of undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione (70 mg, 0.071 mmol) in THF (3 ml) was added acetaldehyde (40% aqueous solution) , 16 mg, 0.142 mmol), the mixture was stirred at room temperature for 30 minutes, then sodium triacetoxyborohydride (75 mg, 0.355 mmol) was added and stirred at room temperature overnight. The reaction solution was diluted with water (15 mL), extracted with DCM (20×3 mL), dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure, the obtained crude product was purified by prep-HPLC to obtain 1-(2-chloro-5-(9- ((4-((1R,4R)-4-(4-(((R)-1-(3-(ethylamino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- Carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1014.3. LC-MS: (ESI, m/z): [M+H] + = 1014.3.
1H NMR(400MHz,DMSO-d 6)δ10.52(s,1H),8.13(s,1H),8.07(s,1H),7.64(d,J＝8.3Hz,1H),7.55(s,1H),7.39(d,J＝8.0Hz,1H),7.00(s,1H),6.90(d,J＝6.5Hz,2H),6.64(s,1H),6.05(s,1H),5.60(t,J＝6.4Hz,1H),3.89(s,3H),3.75-3.40(m,8H),3.11–3.00(m,2H),3.00-2.90(m,1H),2.87-2.70(m,2H),2.70-2.60(m,1H),2.40-2.25(m,7H),2.18-2.07(m,2H),1.90-1.75(m,4H),1.75-1.20(m,18H),1.18-0.96(m,7H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.52(s, 1H), 8.13(s, 1H), 8.07(s, 1H), 7.64(d, J=8.3Hz, 1H), 7.55(s, 1H), 7.39(d, J=8.0Hz, 1H), 7.00(s, 1H), 6.90(d, J=6.5Hz, 2H), 6.64(s, 1H), 6.05(s, 1H), 5.60( t, J＝6.4Hz, 1H), 3.89(s, 3H), 3.75-3.40(m, 8H), 3.11-3.00(m, 2H), 3.00-2.90(m, 1H), 2.87-2.70(m, 2H), 2.70-2.60(m, 1H), 2.40-2.25(m, 7H), 2.18-2.07(m, 2H), 1.90-1.75(m, 4H), 1.75-1.20(m, 18H), 1.18- 0.96(m,7H).
实施例36：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 36: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) yl)phenyl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl yl)piperidine-1-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：5-氨基-2-氯吡啶-4-甲酰胺的制备Step 1: Preparation of 5-amino-2-chloropyridine-4-carboxamide
Figure PCTCN2022088560-appb-000810
Figure PCTCN2022088560-appb-000810
将5-氨基-2-氯吡啶-4-羧酸(14.0g,81.13mmol)用DCM(200mL)溶解，HOBt(13.2g,97.67mmol)和EDCI(18.7g,97.67mmol)加入，常温搅拌1h，加入NH 3H 2O(200mL)搅拌2h，过滤，减压浓缩，得到粗品5-氨基-2-氯吡啶-4-甲酰胺。 5-Amino-2-chloropyridine-4-carboxylic acid (14.0 g, 81.13 mmol) was dissolved in DCM (200 mL), HOBt (13.2 g, 97.67 mmol) and EDCI (18.7 g, 97.67 mmol) were added, and stirred at room temperature for 1 h , NH 3 H 2 O (200 mL) was added and stirred for 2 h, filtered and concentrated under reduced pressure to obtain crude 5-amino-2-chloropyridine-4-carboxamide.
LC-MS:(ESI,m/z):[M+H] +＝172.0. LC-MS: (ESI, m/z): [M+H] + = 172.0.
步骤2：4-(5-氨基-4-氨基甲酰吡啶-2-基)环己-3-烯-1-羧酸甲酯的制备Step 2: Preparation of methyl 4-(5-amino-4-carbamoylpyridin-2-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000811
Figure PCTCN2022088560-appb-000811
将5-氨基-2-氯吡啶-4-甲酰胺(5.0g,29.24mmol)用Dioxane/H 2O(200mL/20ml)解，Cs 2CO 3(47.51g,146.18mmol)，Pd(dppf)Cl 2(2.67g,3.65mmol)和4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯(10.1g,38.1mmol)分别加入，反应液在氮气保护下升温至100℃搅拌过夜，加水(500ml)稀释，用乙酸乙酯(600ml)萃取，无水硫酸钠干燥，减压浓缩，粗产品用柱层析(PE:EA＝1:3)纯化得到4-(5-氨基-4-氨基甲酰吡啶-2-基)环己-3-烯-1-羧酸甲酯。 5-Amino-2-chloropyridine-4-carboxamide (5.0 g, 29.24 mmol) was decomposed with Dioxane/H 2 O (200 mL/20 ml), Cs 2 CO 3 (47.51 g, 146.18 mmol), Pd(dppf) Cl 2 (2.67 g, 3.65 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-en-1- Methyl carboxylate (10.1 g, 38.1 mmol) was added separately, the reaction solution was heated to 100° C. and stirred overnight under nitrogen protection, diluted with water (500 ml), extracted with ethyl acetate (600 ml), dried over anhydrous sodium sulfate, and decompressed. Concentrated, and the crude product was purified by column chromatography (PE:EA=1:3) to give methyl 4-(5-amino-4-carbamoylpyridin-2-yl)cyclohex-3-ene-1-carboxylate .
LC-MS:(ESI,m/z):[M+H] +＝276.0. LC-MS: (ESI, m/z): [M+H] + = 276.0.
步骤3：4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己-3-烯-1-羧酸甲酯的制备Step 3: Preparation of methyl 4-(4-hydroxy-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000812
Figure PCTCN2022088560-appb-000812
将4-(5-氨基-4-氨基甲酰吡啶-2-基)环己-3-烯-1-羧酸甲酯(4.0g,14.55mmol)加入到原乙酸三甲酯(17.46g,145.5mmol)的甲醇(100ml)溶液中，使用闷罐120℃搅拌过夜，冷却后减压浓缩，得到粗产品4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己-3-烯-1-羧酸甲酯。Methyl 4-(5-amino-4-carbamoylpyridin-2-yl)cyclohex-3-ene-1-carboxylate (4.0 g, 14.55 mmol) was added to trimethyl orthoacetate (17.46 g, 145.5 mmol) in methanol (100 ml) solution, stirred overnight at 120°C in a stuffy tank, cooled and concentrated under reduced pressure to obtain the crude product 4-(4-hydroxy-2-methylpyrido[3,4-d]pyrimidine- 6-yl) cyclohex-3-ene-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝300.0. LC-MS: (ESI, m/z): [M+H] + = 300.0.
步骤4：(1R,4R)-4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯的制备Step 4: Preparation of methyl (1R,4R)-4-(4-hydroxy-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000813
Figure PCTCN2022088560-appb-000813
将4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己-3-烯-1-羧酸甲酯(800mg,3.33mmol)和Pd(OH) 2(320mg)加入到甲醇(50mL)溶液中，反应液用氢气置换3次，升温至70℃搅拌过夜，过滤，减压浓缩，粗品用甲醇(40mL)溶解，甲醇钠(1mL,5.4mmol/L)加入，70℃搅拌过夜，H 2SO 4调节pH至3-4，50℃搅拌过夜，减压浓缩，通过反相制备纯化得到(1R,4R)-4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯。 4-(4-Hydroxy-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester (800 mg, 3.33 mmol) and Pd(OH ) 2 (320 mg) was added to methanol (50 mL) solution, the reaction solution was replaced with hydrogen 3 times, heated to 70 ° C and stirred overnight, filtered, concentrated under reduced pressure, the crude product was dissolved in methanol (40 mL), sodium methoxide (1 mL, 5.4 mmol) /L) was added, stirred at 70 °C overnight, adjusted to pH 3-4 with H 2 SO 4 , stirred at 50 °C overnight, concentrated under reduced pressure, and purified by reverse-phase preparation to obtain (1R,4R)-4-(4-hydroxy-2 -methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝302.1. LC-MS: (ESI, m/z): [M+H] + = 302.1.
步骤5：(1R,4R)-4-(2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯的制备Step 5: (1R,4R)-4-(2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)pyrido[3,4-d]pyrimidine Preparation of -6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000814
Figure PCTCN2022088560-appb-000814
将2,4,6-三异丙基苯基磺酰氯(1.0g,3.3mmol)和DMAP(20.3mg,0.165mmol)，TEA(503mg,4.98mmol)加入到(1R,4R)-4-(4-羟基-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯(500mg,1.66mmol)的二氯甲烷(30ml)溶液中，常温搅拌过夜，用水(50ml)和饱和食盐水(40mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，通过柱层析(PE:EA＝1:3)纯化得到(1R,4R)-4-(2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯。2,4,6-Triisopropylphenylsulfonyl chloride (1.0 g, 3.3 mmol) and DMAP (20.3 mg, 0.165 mmol), TEA (503 mg, 4.98 mmol) were added to (1R,4R)-4-( A solution of methyl 4-hydroxy-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carboxylate (500mg, 1.66mmol) in dichloromethane (30ml) at room temperature After stirring overnight, the organic phase was washed with water (50 mL) and saturated brine (40 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and purified by column chromatography (PE:EA=1:3) to obtain (1R,4R) )-4-(2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane Methyl alkane-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝568.2. LC-MS: (ESI, m/z): [M+H] + = 568.2.
步骤6：(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯的制备Step 6: (1R,4R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3, Preparation of methyl 4-d]pyrimidin-6-yl)cyclohexane-1-carboxylate
Figure PCTCN2022088560-appb-000815
Figure PCTCN2022088560-appb-000815
将(1R,4R)-4-(2-甲基-4-(((2,4,6-三异丙基苯基)磺酰基)氧)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯(800mg,1.41mmol)和TEA(546.1mg,4.23mmol)加入到1-(3-硝基-5-(三氟甲基)苯基)乙基-1-胺(462mg,1.97mmol)的DMSO(20mL)溶液中，室温搅拌过夜，粗品使用反相柱层析(ACN/H 2O＝2/1)纯化得到(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯。 (1R,4R)-4-(2-methyl-4-(((2,4,6-triisopropylphenyl)sulfonyl)oxy)pyrido[3,4-d]pyrimidine-6 -yl)cyclohexane-1-carboxylate methyl ester (800 mg, 1.41 mmol) and TEA (546.1 mg, 4.23 mmol) were added to 1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl A solution of yl-1-amine (462 mg, 1.97 mmol) in DMSO (20 mL) was stirred at room temperature overnight, and the crude product was purified by reverse-phase column chromatography (ACN/H 2 O=2/1) to give (1R,4R)-4 -(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl) Methyl cyclohexane-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝518.4. LC-MS: (ESI, m/z): [M+H] + = 518.4.
步骤7：(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸的制备Step 7: (1R,4R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3, Preparation of 4-d]pyrimidin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000816
Figure PCTCN2022088560-appb-000816
将(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸甲酯(400mg,0.774mmol)溶解在THF/H 2O(40ml/10ml)溶液中，加入LiOH(93mg,3.87mmol)，反应液升温至50℃搅拌过夜，用HCl(1M)调节pH至中性，加水(50ml)溶解，用乙酸乙酯(100ml)萃取，减压浓缩，得到粗品(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸。 (1R,4R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4- d]Methyl pyrimidin-6-yl)cyclohexane-1-carboxylate (400mg, 0.774mmol) was dissolved in THF/H 2 O (40ml/10ml) solution, added LiOH (93mg, 3.87mmol), the reaction solution The temperature was raised to 50°C and stirred overnight, adjusted to neutral pH with HCl (1M), dissolved in water (50ml), extracted with ethyl acetate (100ml), and concentrated under reduced pressure to obtain crude product (1R,4R)-4-(2- Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane- 1-Carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝504.2. LC-MS: (ESI, m/z): [M+H] + = 504.2.
步骤8：1-(2-甲氧基-5-(4-((2-(1-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶 并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 8: 1-(2-Methoxy-5-(4-((2-(1-((1R,4R)-4-(2-methyl-4-((((R)-1-() 3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl )ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000817
Figure PCTCN2022088560-appb-000817
将(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸(180mg,0.357mmol)，HATU(203.5mg,0.536mmol)和DIEA(138.2mg,1.07mmol)加入到1-(2-甲氧基-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的DMF(6ml)溶液中，室温搅拌过夜，加水(50ml)溶解，用二氯甲烷(30ml×3)萃取，减压浓缩，粗品使用反相柱层析(ACN/H 2O＝1/2)纯化得到1-(2-甲氧基-5-(4-((2-(1-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (1R,4R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4- d] pyrimidin-6-yl)cyclohexane-1-carboxylic acid (180 mg, 0.357 mmol), HATU (203.5 mg, 0.536 mmol) and DIEA (138.2 mg, 1.07 mmol) were added to 1-(2-methoxyl -5-(4-((2-(Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione in DMF (6ml) solution, stirred overnight at room temperature, dissolved in water (50ml), extracted with dichloromethane (30ml×3), concentrated under reduced pressure, and the crude product was subjected to reverse-phase column chromatography (ACN/H 2 O=1/2 ) was purified to give 1-(2-methoxy-5-(4-((2-(1-((1R,4R)-4-(2-methyl-4-((((R)-1-() 3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl )ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝958.5. LC-MS: (ESI, m/z): [M+H] + = 958.5.
步骤9：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 9: 1-(5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) )phenyl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl ) piperidine-1-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione preparation
Figure PCTCN2022088560-appb-000818
Figure PCTCN2022088560-appb-000818
将1-(2-甲氧基-5-(4-((2-(1-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(300mg,0.313mmol)溶于乙醇(20ml)，Raney-Ni(aq.,1mL)，水合肼(0.5mL)加入，反应液室温搅拌1小时,过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Methoxy-5-(4-((2-(1-((1R,4R)-4-(2-methyl-4-((((R)-1-(3- Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethyl Oxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (300mg, 0.313mmol) was dissolved in ethanol (20ml), Raney-Ni (aq. , 1 mL), hydrazine hydrate (0.5 mL) was added, the reaction solution was stirred at room temperature for 1 hour, filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(4-((2-(1-((1R ,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylpyrido[3,4- d] pyrimidin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-methoxyphenyl)dihydropyrimidine- 2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝928.5. LC-MS: (ESI, m/z): [M+H] + = 928.5.
1H NMR(400MHz,DMSO-d 6)δ10.33(s,1H),8.91(s,1H),8.58(d,J＝7.9Hz,1H),8.10(s,1H),7.36(dd,J＝8.4,1.9Hz,1H),7.32(d,J＝1.9Hz,1H),7.15(d,J＝8.5Hz,1H),6.89(s,1H),6.85(s,1H),6.71(s,1H),5.57–5.51(m,3H),4.45-4.33(m,1H),4.00-3.90(m,1H),3.84(s,3H),3.59(t,J＝6.6Hz,2H),3.41(t,J＝6.2Hz,2H),3.24(d,J＝6.2Hz,2H),3.05-2.95(m,2H),2.83-2.70(m,2H),2.70-2.65(m,3H),2.43(s,3H),2.05-1.96(m,2H),1.88-1.40(m,20H),1.23-0.89(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.33(s, 1H), 8.91(s, 1H), 8.58(d, J=7.9Hz, 1H), 8.10(s, 1H), 7.36(dd, J=8.4, 1.9Hz, 1H), 7.32(d, J=1.9Hz, 1H), 7.15(d, J=8.5Hz, 1H), 6.89(s, 1H), 6.85(s, 1H), 6.71( s, 1H), 5.57-5.51(m, 3H), 4.45-4.33(m, 1H), 4.00-3.90(m, 1H), 3.84(s, 3H), 3.59(t, J=6.6Hz, 2H) ,3.41(t,J＝6.2Hz,2H),3.24(d,J＝6.2Hz,2H),3.05-2.95(m,2H),2.83-2.70(m,2H),2.70-2.65(m,3H) ),2.43(s,3H),2.05-1.96(m,2H),1.88-1.40(m,20H),1.23-0.89(m,4H).
实施例37：1-(5-(2-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-基)-2-氧代乙氧基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 37: 1-(5-(2-(4-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine- 1-yl)-2-oxoethoxy)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(哌啶-4-基甲基)哌嗪-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(piperidin-4-ylmethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000819
Figure PCTCN2022088560-appb-000819
将4-((1-((苄氧基)羰基)哌啶-4-基)甲基)哌嗪-1-羧酸叔丁酯(500mg,1.20mmol)和Pd/C(100mg)在MeOH(10mL)中的混合物在室温H 2氛围下搅拌2.0h。反应液过滤，减压浓缩得到4-(哌啶-4-基甲基)哌嗪-1-羧酸叔丁酯。 Combine tert-butyl 4-((1-(((benzyloxy)carbonyl)piperidin-4-yl)methyl)piperazine-1-carboxylate (500 mg, 1.20 mmol) and Pd/C (100 mg) in MeOH The mixture in (10 mL) was stirred at room temperature under H2 atmosphere for 2.0 h. The reaction solution was filtered and concentrated under reduced pressure to obtain tert-butyl 4-(piperidin-4-ylmethyl)piperazine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝284.1. LC-MS: (ESI, m/z): [M+H] + = 284.1.
步骤2：4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羧酸叔丁酯的制备Step 2: 4-((1-(2-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenoxy)acetyl)piperidine-4- Preparation of tert-butyl)methyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000820
Figure PCTCN2022088560-appb-000820
将2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酸(240mg,0.805mmol)，4-(哌啶-4-基甲基)哌嗪-1-羧酸叔丁酯(251mg,0.886mmol)，HATU(612mg,1.61mmol)和DIEA(312mg,2.42mmol)在DMF(5mL)中的混合物在室温搅拌3h。反应加水(20mL)淬灭，DCM(20mL×2)萃取，分离有机相，用无水Na 2SO 4干燥，过滤，减压浓缩。粗品经层析柱(MeOH:DCM＝0-1:24))纯化得到4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羧酸叔丁酯。 2-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenoxy)acetic acid (240 mg, 0.805 mmol), 4-(piperidin-4-yl A mixture of methyl)piperazine-1-carboxylate tert-butyl ester (251 mg, 0.886 mmol), HATU (612 mg, 1.61 mmol) and DIEA (312 mg, 2.42 mmol) in DMF (5 mL) was stirred at room temperature for 3 h. The reaction was quenched with water (20 mL), extracted with DCM (20 mL x 2), the organic phase was separated, dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (MeOH:DCM=0-1:24)) to give 4-((1-(2-(4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H) )-yl)phenoxy)acetyl)piperidin-4-yl)methyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝564.2. LC-MS: (ESI, m/z): [M+H] + = 564.2.
步骤3：1-(2-氯-5-(2-氧代-2-(4-(哌嗪-1-基甲基)哌啶-1-基)乙氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(2-oxo-2-(4-(piperazin-1-ylmethyl)piperidin-1-yl)ethoxy)phenyl)dihydropyrimidine Preparation of -2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000821
Figure PCTCN2022088560-appb-000821
将4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羧酸叔丁酯(350mg,0.622mmol)的TFA/DCM(10mL/3mL)混合物在室温搅拌2h。反应液直接浓缩得到1-(2-氯-5-(2-氧代-2-(4-(哌嗪-1-基甲基)哌啶-1-基)乙氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-((1-(2-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenoxy)acetyl)piperidin-4-yl) A mixture of methyl)piperazine-1-carboxylate tert-butyl ester (350 mg, 0.622 mmol) in TFA/DCM (10 mL/3 mL) was stirred at room temperature for 2 h. The reaction solution was directly concentrated to obtain 1-(2-chloro-5-(2-oxo-2-(4-(piperazin-1-ylmethyl)piperidin-1-yl)ethoxy)phenyl)di Hydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝464.2. LC-MS: (ESI, m/z): [M+H] + = 464.2.
步骤4：(3-((R)-1-((6-((1R,4R)-4-(4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 4: (3-((R)-1-((6-((1R,4R)-4-(4-((1-(2-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)phenoxy)acetyl)piperidin-4-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Preparation of quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000822
Figure PCTCN2022088560-appb-000822
向1-(2-氯-5-(2-氧代-2-(4-(哌嗪-1-基甲基)哌啶-1-基)乙氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(260mg,0.562mmol)，HATU(426mg,1.12mmol)和DIEA(217mg,3.36mmol)的DMF(3mL)溶液中加入(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(405.6mg,0.674mmol)。然后反应液在室温搅拌1h。反应液中加水(20mL)淬灭反应，DCM(20mL×2)萃取，有机相经无水Na 2SO 4干燥，过滤，减压浓缩。粗品经柱层析(MeOH:DCM＝0-2:23))纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。 To 1-(2-chloro-5-(2-oxo-2-(4-(piperazin-1-ylmethyl)piperidin-1-yl)ethoxy)phenyl)dihydropyrimidine-2 , 4(1H,3H)-dione (260 mg, 0.562 mmol), HATU (426 mg, 1.12 mmol) and DIEA (217 mg, 3.36 mmol) in DMF (3 mL) was added (1R,4R)-4-(4 -(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carboxylic acid (405.6 mg, 0.674 mmol). The reaction solution was then stirred at room temperature for 1 h. Water (20 mL) was added to the reaction solution to quench the reaction, extracted with DCM (20 mL×2), the organic phase was dried over anhydrous Na 2 SO 4 , filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (MeOH:DCM=0-2:23)) to give (3-((R)-1-((6-((1R,4R)-4-(4-((1-( 2-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenoxy)acetyl)piperidin-4-yl)methyl)piperazine-1- Carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1048.6. LC-MS: (ESI, m/z): [M+H] + = 1048.6.
步骤5：1-(5-(2-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-基)-2-氧代乙氧基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(5-(2-(4-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidine-1 Preparation of -yl)-2-oxoethoxy)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000823
Figure PCTCN2022088560-appb-000823
将(3-((R)-1-((6-((1R,4R)-4-(4-((1-(2-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯氧基)乙酰基)哌啶-4-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(140mg,0.13mmol)的DCM/TFA(3mL/1mL)溶液在室温下搅拌2h。反应液直接减压浓缩，所得粗品经Prep-HPLC(乙腈/0.05％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-(2-(4-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)哌啶-1-基)-2-氧代乙氧基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-((1-(2-(4-Chloro-3-(2,4-dioxotetra) Hydropyrimidin-1(2H)-yl)phenoxy)acetyl)piperidin-4-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazole Lin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (140 mg, 0.13 mmol) in DCM/TFA (3 mL/1 mL) was stirred at room temperature for 2 h. The reaction solution was directly concentrated under reduced pressure, and the obtained crude product was purified by Prep-HPLC (acetonitrile/0.05% NH 4 HCO 3 aqueous solution, 5%~95%) to obtain 1-(5-(2-(4-((4-((1R ,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)piperidin-1-yl)-2-oxoethoxy)-2-chlorophenyl)dihydro Pyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝948.4. LC-MS: (ESI, m/z): [M+H] + = 948.4.
1H NMR(400MHz,DMSO-d 6)δ10.47(s,1H),8.24-7.87(m,2H),7.45(d,J＝8.9Hz,1H),7.11(d,J＝2.9Hz,1H),6.99(s,1H),6.93(dd,J＝9.0,3.0Hz,1H),6.86(d,J＝10.9Hz,2H),6.70(s,1H),5.67-5.40(m,3H),4.93–4.63(m,2H),4.40-4.24(m,1H),3.89(s,3H),3.82-3.65(m,2H),3.63-3.42(m,4H),3.09-2.89(m,2H),2.77-2.55(m,5H),2.41-2.25(m,7H),2.12(d,J＝6.5Hz,2H),1.9-1.48(m,14H),1.15-0.88(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ10.47(s,1H),8.24-7.87(m,2H),7.45(d,J=8.9Hz,1H),7.11(d,J=2.9Hz, 1H), 6.99(s, 1H), 6.93(dd, J=9.0, 3.0Hz, 1H), 6.86(d, J=10.9Hz, 2H), 6.70(s, 1H), 5.67-5.40(m, 3H) ), 4.93-4.63(m, 2H), 4.40-4.24(m, 1H), 3.89(s, 3H), 3.82-3.65(m, 2H), 3.63-3.42(m, 4H), 3.09-2.89(m ,2H),2.77-2.55(m,5H),2.41-2.25(m,7H),2.12(d,J=6.5Hz,2H),1.9-1.48(m,14H),1.15-0.88(m,2H ).
实施例38：1-(5-((4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-基)甲基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 38: 1-(5-((4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoro) Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl) yl)amino)piperidin-1-yl)methyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：1-(2-氯-5-(羟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 1: Preparation of 1-(2-Chloro-5-(hydroxymethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000824
Figure PCTCN2022088560-appb-000824
4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(2.0g,4.61mmol)溶解于无水四氢呋喃中(40mL)，氮气保护下降温至-60℃，边搅拌边向上述溶液中滴加氢化铝锂的四氢呋喃溶液(9.22mL,1.0mmol/L)。加完后-60℃下搅拌1小时后，向反应液中滴加饱和氯化铵水溶液(20mL)，过滤，母液用乙酸乙酯(30mLx3)提取。有机相用饱和食盐水(100mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到1-(2-氯-5-(羟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。Pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (2.0 g, 4.61 mmol) was dissolved in anhydrous tetrahydrofuran (40 mL) under nitrogen protection The temperature was lowered to -60°C, and a solution of lithium aluminum hydride in tetrahydrofuran (9.22 mL, 1.0 mmol/L) was added dropwise to the above solution while stirring. After the addition, the mixture was stirred at -60°C for 1 hour, and then a saturated aqueous ammonium chloride solution (20 mL) was added dropwise to the reaction solution, filtered, and the mother liquor was extracted with ethyl acetate (30 mL×3). The organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (methanol:dichloromethane=1:9) to obtain 1-(2-chloro-5-(hydroxymethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione .
LC-MS:(ESI,m/z):[M+H] +＝255.0 LC-MS: (ESI, m/z): [M+H] + = 255.0
步骤2：4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲醛的制备Step 2: Preparation of 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzaldehyde
Figure PCTCN2022088560-appb-000825
Figure PCTCN2022088560-appb-000825
1-(2-氯-5-(羟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(450mg,1.76mmol)用乙腈(20mL)溶解，加入IBX(988mg,3.53mmol)并升温至80℃搅拌1小时。反应液过滤，滤饼用甲醇(20mLx3)洗涤，滤液减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲醛。1-(2-Chloro-5-(hydroxymethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (450 mg, 1.76 mmol) was dissolved in acetonitrile (20 mL), IBX (988 mg, 1.76 mmol) was added. 3.53 mmol) and warmed to 80 °C and stirred for 1 hour. The reaction solution was filtered, the filter cake was washed with methanol (20 mL×3), the filtrate was concentrated under reduced pressure, and the crude product was purified by column chromatography (methanol:dichloromethane=1:9) to obtain 4-chloro-3-(2,4-dioxo) tetrahydropyrimidin-1(2H)-yl)benzaldehyde.
LC-MS:(ESI,m/z):[M+H] +＝253.0. LC-MS: (ESI, m/z): [M+H] + = 253.0.
1H NMR(400MHz,DMSO-d 6)δ10.57(s,1H),10.01(s,1H),8.06(d,J＝1.8Hz,1H),7.93(dd,J＝8.2,1.9Hz,1H),7.84(d,J＝8.2Hz,1H),3.80(dd,J＝16.6,9.3Hz,1H),3.64(dt,J＝12.1,6.1Hz,1H),2.77(dd,J＝12.5,6.4Hz,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.57 (s, 1H), 10.01 (s, 1H), 8.06 (d, J=1.8Hz, 1H), 7.93 (dd, J=8.2, 1.9Hz, 1H),7.84(d,J=8.2Hz,1H),3.80(dd,J=16.6,9.3Hz,1H),3.64(dt,J=12.1,6.1Hz,1H),2.77(dd,J=12.5 ,6.4Hz,2H).
步骤3：4-(3-氧代丙基)哌啶-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(3-oxopropyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000826
Figure PCTCN2022088560-appb-000826
将4-(3-羟丙基)哌啶-1-羧酸叔丁酯(500mg,2.05mmol)溶解于乙腈(20mL)中，加入IBX(1.15g，4.11mmol)并升温至70℃搅拌1小时。反应液过滤，滤饼用甲醇(20mLx3)洗涤，滤液减压浓缩，粗品使用柱层析(乙酸乙酯:石油醚＝1:1)纯化得到4-(3-氧代丙基)哌啶-1-羧酸叔丁酯。4-(3-Hydroxypropyl)piperidine-1-carboxylate tert-butyl ester (500 mg, 2.05 mmol) was dissolved in acetonitrile (20 mL), IBX (1.15 g, 4.11 mmol) was added and the temperature was raised to 70 °C and stirred for 1 Hour. The reaction solution was filtered, the filter cake was washed with methanol (20 mL×3), the filtrate was concentrated under reduced pressure, and the crude product was purified by column chromatography (ethyl acetate:petroleum ether=1:1) to obtain 4-(3-oxopropyl)piperidine- 1-Carboxylic acid tert-butyl ester.
1H NMR(400MHz,DMSO-d 6)δ9.68(t,J＝1.5Hz,1H),3.91(d,J＝12.0Hz,2H),2.65(m,2H),2.46(td,J＝7.5,1.5Hz,2H),1.61(d,J＝13.0Hz,2H),1.46(2H),1.42–1.33(m,10H),0.94(2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 9.68 (t, J=1.5Hz, 1H), 3.91 (d, J=12.0Hz, 2H), 2.65 (m, 2H), 2.46 (td, J= 7.5,1.5Hz,2H),1.61(d,J=13.0Hz,2H),1.46(2H),1.42–1.33(m,10H),0.94(2H).
步骤4：4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯的制备Step 4: Preparation of benzyl 4-((3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000827
Figure PCTCN2022088560-appb-000827
4-(3-氧代丙基)哌啶-1-羧酸叔丁酯(300mg,1.2mmol)和4-(甲氨基)哌啶-1-羧酸苄酯(308mg,1.2mmol)用四氢呋喃(20mL)溶解，搅拌下加入三乙酰氧基硼氢化钠(1.2g,6.0mmol)。室温下搅拌2小时后，加水(50mL)，用二氯甲烷(30mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯。4-(3-Oxopropyl)piperidine-1-carboxylate tert-butyl ester (300mg, 1.2mmol) and 4-(methylamino)piperidine-1-carboxylate benzyl ester (308mg, 1.2mmol) were treated with tetrahydrofuran (20 mL) was dissolved, and sodium triacetoxyborohydride (1.2 g, 6.0 mmol) was added with stirring. After stirring at room temperature for 2 hours, water (50 mL) was added, extracted with dichloromethane (30 mL×3), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography ( Methanol:dichloromethane=1:9) purification to give 4-((3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylic acid benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝474.3. LC-MS: (ESI, m/z): [M+H] + = 474.3.
步骤5：4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羧酸叔丁酯的制备Step 5: Preparation of tert-butyl 4-(3-(methyl(piperidin-4-yl)amino)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000828
Figure PCTCN2022088560-appb-000828
4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯(400mg,0.84mmol)溶于EA(20mL)中，加入Pd(OH) 2/C(200mg,0.28mmol)，在氢气氛围下升温至70℃并搅拌过夜。反应液冷却至室温，过滤，滤液减压浓缩得到4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羧酸叔丁酯。粗品无需纯化直接用于下一步反应。 Benzyl 4-((3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylate (400 mg, 0.84 mmol) was dissolved in EA ( 20 mL), Pd(OH) 2 /C (200 mg, 0.28 mmol) was added, the temperature was raised to 70° C. under a hydrogen atmosphere, and the mixture was stirred overnight. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain tert-butyl 4-(3-(methyl(piperidin-4-yl)amino)propyl)piperidine-1-carboxylate. The crude product was used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝340.3. LC-MS: (ESI, m/z): [M+H] + = 340.3.
步骤6：4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羧酸叔丁酯的制备Step 6: 4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenyl)piperidin-4-yl)(methyl Preparation of tert-butyl)amino)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000829
Figure PCTCN2022088560-appb-000829
4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羧酸叔丁酯(280mg,0.82mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲醛(311mg,1.23mmol)用四氢呋喃(20mL)溶解，加入三乙酰氧基硼氢化钠(869mg,4.1mmol)。反应液升温至50℃并搅拌2小时，加水(50mL)稀释，用二氯甲烷(30mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羧酸叔丁酯。4-(3-(Methyl(piperidin-4-yl)amino)propyl)piperidine-1-carboxylate tert-butyl ester (280 mg, 0.82 mmol) and 4-chloro-3-(2,4-di Oxotetrahydropyrimidin-1(2H)-yl)benzaldehyde (311 mg, 1.23 mmol) was dissolved in tetrahydrofuran (20 mL) and sodium triacetoxyborohydride (869 mg, 4.1 mmol) was added. The reaction solution was heated to 50 °C and stirred for 2 hours, diluted with water (50 mL), extracted with dichloromethane (30 mL×3), washed with saturated brine (100 mL), and the organic phase was washed with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product Purification using column chromatography (methanol:dichloromethane=1:9) gave 4-(3-((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)- yl)phenyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝576.2. LC-MS: (ESI, m/z): [M+H] + = 576.2.
步骤7：1-(2-氯-5-((4-(甲基(3-(哌啶-4-基)丙基)氨基)-1-基)甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(2-Chloro-5-((4-(methyl(3-(piperidin-4-yl)propyl)amino)-1-yl)methyl)phenyl)dihydropyrimidine- Preparation of 2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000830
Figure PCTCN2022088560-appb-000830
4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羧酸叔丁酯(180mg,0.31mmol)用二氯甲烷(5mL)溶解，三氟乙酸(2mL)加入并室温搅拌2小时，直接减压浓缩得到1-(2-氯-5-((4-(甲基(3-(哌啶-4-基)丙基)氨基)-1-基)甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，无需纯化直接用于下一步反应。4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenyl)piperidin-4-yl)(methyl)amino )propyl)piperidine-1-carboxylate tert-butyl ester (180mg, 0.31mmol) was dissolved in dichloromethane (5mL), trifluoroacetic acid (2mL) was added and stirred at room temperature for 2 hours, directly concentrated under reduced pressure to obtain 1-( 2-Chloro-5-((4-(methyl(3-(piperidin-4-yl)propyl)amino)-1-yl)methyl)phenyl)dihydropyrimidine-2,4(1H, 3H)-diketone was used in the next step without purification.
LC-MS:(ESI,m/z):[M+H] +＝476.3. LC-MS: (ESI, m/z): [M+H] + = 476.3.
步骤8：(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 8: (3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)phenyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2- Preparation of methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000831
Figure PCTCN2022088560-appb-000831
1-(2-氯-5-((4-(甲基(3-(哌啶-4-基)丙基)氨基)-1-基)甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(180mg,0.31mmol)溶于DMF(10mL)中，加入(1R,4R)-4-(4-(((R)-1-(3-(叔丁氧羰基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.24mmol)，HATU(118mg,0.31mmol)和N,N-二异丙基乙胺(93mg,0.72mmol)，室温下搅拌2h，加水(100mL)，用乙酸乙酯(30mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。1-(2-Chloro-5-((4-(methyl(3-(piperidin-4-yl)propyl)amino)-1-yl)methyl)phenyl)dihydropyrimidine-2,4 (1H,3H)-dione (180 mg, 0.31 mmol) was dissolved in DMF (10 mL), (1R,4R)-4-(4-(((R)-1-(3-(tert-butoxycarbonyl) was added ) amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.24 mmol), HATU (118 mg, 0.31 mmol) and N,N-di Isopropylethylamine (93 mg, 0.72 mmol), stirred at room temperature for 2 h, added water (100 mL), extracted with ethyl acetate (30 mL×3), washed the organic phase with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, Concentrated under reduced pressure, the crude product was purified by column chromatography (methanol:dichloromethane=1:9) to obtain (3-((R)-1-((6-((1R,4R)-4-(4-(3 -((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)phenyl)piperidin-4-yl)(methyl)amino)propyl) Piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1060.5. LC-MS: (ESI, m/z): [M+H] + = 1060.5.
步骤9：1-(5-((4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-基)甲基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 9: 1-(5-((4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl ) amino)piperidin-1-yl)methyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione preparation
Figure PCTCN2022088560-appb-000832
Figure PCTCN2022088560-appb-000832
(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯基)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(200mg,0.19mmol)用二氯甲烷(5mL)溶解，加入三氟乙酸(2mL)，室温搅拌2小时后，反应液减压浓缩，所得油状物用10％甲醇/二氯甲烷混合溶液(20mL)溶解，加入5％碳酸氢钠水溶液(20mL)并搅拌1小时，分离所得有机相经无水硫酸钠干燥，过滤，减压浓缩得到粗品，粗品经Pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-((4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-基)甲基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydro) Pyrimidine-1(2H)-yl)phenyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinoline Zolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (200 mg, 0.19 mmol) was dissolved in dichloromethane (5 mL), trifluoroacetic acid (2 mL) was added ), after stirring at room temperature for 2 hours, the reaction solution was concentrated under reduced pressure, the obtained oil was dissolved in a 10% methanol/dichloromethane mixed solution (20 mL), 5% aqueous sodium bicarbonate solution (20 mL) was added and stirred for 1 hour, the obtained organic The phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain the crude product, which was purified by Pre-HPLC (CH 3 CN/0.08% NH 4 HCO 3 aqueous solution, 5%-95%) to obtain 1-(5-((4 -((3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidin-1-yl)methyl yl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝960.5. LC-MS: (ESI, m/z): [M+H] + = 960.5.
1H NMR(400MHz,DMSO-d 6)δ10.45(s,1H),8.16–8.02(m,2H),7.50(d,J＝8.2Hz,1H),7.38(s,1H), 7.29(d,J＝8.3Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.64–5.47(m,3H),4.45-4.35(m,1H),3.96-3.85(m,4H),3.76–3.54(m,2H),3.47-3.40(m,2H),3.08-2.90(m,2H),2.89-2.77(m,2H),2.77-2.60(m,3H),2.35(s,6H),2.15(s,3H),1.98-1.40(m,23H),1.24-1.18(m,2H),1.08-0.82(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.45(s, 1H), 8.16-8.02(m, 2H), 7.50(d, J=8.2Hz, 1H), 7.38(s, 1H), 7.29( d, J＝8.3Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.64-5.47(m, 3H), 4.45-4.35 (m,1H),3.96-3.85(m,4H),3.76-3.54(m,2H),3.47-3.40(m,2H),3.08-2.90(m,2H),2.89-2.77(m,2H) ,2.77-2.60(m,3H),2.35(s,6H),2.15(s,3H),1.98-1.40(m,23H),1.24-1.18(m,2H),1.08-0.82(m,2H) .
实施例39：5-(4-((2-(1-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(2,6-二氧代哌啶-3-基)异吲哚啉-1,3-二酮步骤1：2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸的制备Example 39: 5-(4-((2-(1-((1S,4S)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene)) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine -1-Carbonyl)-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione Step 1: 2-(2,6-dioxopiperidine- Preparation of 3-yl)-1,3-dioxoisoindoline-5-carboxylic acid
Figure PCTCN2022088560-appb-000833
Figure PCTCN2022088560-appb-000833
将1,3-二氧代-1,3-二氢异苯并呋喃-5-羧酸(1.0g,5.21mmol)用AcOH(10ml)溶解，乙酸钾(945mg,5.73mmol)和3-氨基哌啶-2,6-二酮盐酸盐(945mg,5.73mmol)加入，反应液加热到90℃搅拌过夜，减压浓缩，水(20mL)加入到粗品中，搅拌10分钟，过滤，滤饼用水洗涤(10mL×3)，真空干燥得到粗品2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸。1,3-Dioxo-1,3-dihydroisobenzofuran-5-carboxylic acid (1.0 g, 5.21 mmol) was dissolved in AcOH (10 ml), potassium acetate (945 mg, 5.73 mmol) and 3-amino Piperidine-2,6-dione hydrochloride (945 mg, 5.73 mmol) was added, the reaction solution was heated to 90 °C and stirred overnight, concentrated under reduced pressure, water (20 mL) was added to the crude product, stirred for 10 minutes, filtered, and the filter cake Washed with water (10 mL×3) and dried in vacuo to obtain crude 2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝303.0. LC-MS: (ESI, m/z): [M+H] + = 303.0.
步骤2：2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸五氟苯酯的制备Step 2: Preparation of 2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carboxylic acid pentafluorophenyl ester
Figure PCTCN2022088560-appb-000834
Figure PCTCN2022088560-appb-000834
将2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸(1.4g,4.64mmol)用DMF(20ml)溶解，DCC(1.43g,6.96mmol)和2,3,4,5,6-五氟苯酚(1.30g,6.96mmol)加入，反应液室温下搅拌过夜，用水(150mL)稀释，乙酸乙酯(100ml×3)萃取，无水硫酸钠干燥，减压浓缩，粗产品通过柱层析(PE:EA＝1:1)纯化得到2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸五氟苯酯。2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carboxylic acid (1.4g, 4.64mmol) was dissolved in DMF (20ml), DCC (1.43g, 6.96mmol) and 2,3,4,5,6-pentafluorophenol (1.30g, 6.96mmol) were added, the reaction solution was stirred at room temperature overnight, diluted with water (150mL), ethyl acetate (100ml×3 ) extraction, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:1) to obtain 2-(2,6-dioxopiperidin-3-yl)-1, 3-dioxoisoindoline-5-carboxylic acid pentafluorophenyl ester.
1H NMR(400MHz,DMSO-d 6)δ11.16(s,1H),8.41(dd,J＝7.8,1.3Hz,1H),8.28(s,1H),8.06(d,J＝7.8Hz,1H),5.20(dd,J＝12.8,5.4Hz,1H),2.66–2.47(m,5H). 1 H NMR (400MHz, DMSO-d 6 ) δ 11.16 (s, 1H), 8.41 (dd, J=7.8, 1.3 Hz, 1H), 8.28 (s, 1H), 8.06 (d, J=7.8 Hz, 1H), 5.20(dd, J=12.8, 5.4Hz, 1H), 2.66–2.47(m, 5H).
步骤3：4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 3: 4-(2-((1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carbonyl)piperidine- Preparation of 4-yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000835
Figure PCTCN2022088560-appb-000835
将2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羧酸五氟苯酯(480mg,1.02mmol)加入到4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(400mg,1.22mmol)的DMSO(10mL)中，室温下搅拌过夜，用水(50mL)稀释，乙酸乙酯(30mL×3)萃取，无水硫酸钠干燥，减压浓缩，粗产品通过柱层析(PE:EA＝1:10)纯化得到4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carboxylic acid pentafluorophenyl ester (480 mg, 1.02 mmol) was added to 4-( 2-(Piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (400 mg, 1.22 mmol) in DMSO (10 mL), stirred at room temperature overnight, diluted with water (50 mL), Ethyl acetate (30 mL×3) was extracted, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:10) to obtain 4-(2-((1-(2-( 2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1- tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝611.3. LC-MS: (ESI, m/z): [M+H] + = 611.3.
步骤4：2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)异吲哚啉-1,3-二酮的制备Step 4: 2-(2,6-Dioxopiperidin-3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1- Preparation of carbonyl)isoindoline-1,3-dione
Figure PCTCN2022088560-appb-000836
Figure PCTCN2022088560-appb-000836
将4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯(250mg,0.41mmol)用DCM(5mL)溶解，三氟乙酸(1mL)加入，反应液室温搅拌过夜,减压浓缩得到粗品2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)异吲哚啉-1,3-二酮。4-(2-((1-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindoline-5-carbonyl)piperidine-4- tert-butyl) methoxy)ethyl)piperidine-1-carboxylate (250 mg, 0.41 mmol) was dissolved in DCM (5 mL), trifluoroacetic acid (1 mL) was added, the reaction solution was stirred at room temperature overnight, and concentrated under reduced pressure to obtain Crude 2-(2,6-dioxopiperidin-3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl) Isoindoline-1,3-dione.
LC-MS:(ESI,m/z):[M+H] +＝511.3. LC-MS: (ESI, m/z): [M+H] + = 511.3.
步骤5：(3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 5: (3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-dioxopiperidine- 3-yl)-1,3-dioxoisoindoline-5-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy Preparation of tert-butyl-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000837
Figure PCTCN2022088560-appb-000837
将2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)异吲哚啉-1,3-二酮(200mg,0.40mmol)，HATU(130mg,0.35mmol)和DIEA(89mg,0.69mmol)加入到(1S,4S)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(140mg,0.23mmol)的DMF(10mL)中，反应液室温搅拌2小时，用水(50mL)稀释，搅拌10分钟，过滤，固体用水洗涤(5mL×2)，得到粗产品(3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。2-(2,6-dioxopiperidin-3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl) Isoindoline-1,3-dione (200 mg, 0.40 mmol), HATU (130 mg, 0.35 mmol) and DIEA (89 mg, 0.69 mmol) were added to (1S,4S)-4-(4-((((R )-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline-6- base) cyclohexane-1-carboxylic acid (140 mg, 0.23 mmol) in DMF (10 mL), the reaction solution was stirred at room temperature for 2 hours, diluted with water (50 mL), stirred for 10 minutes, filtered, and the solid was washed with water (5 mL×2) , to obtain the crude product (3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-dioxopiperidine) -3-yl)-1,3-dioxoisoindoline-5-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methyl Oxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1095.5. LC-MS: (ESI, m/z): [M+H] + = 1095.5.
步骤6：5-(4-((2-(1-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(2,6-二氧代哌啶-3-基)异吲哚啉-1,3-二酮的制备Step 6: 5-(4-((2-(1-((1S,4S)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine- Preparation of 1-carbonyl)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
Figure PCTCN2022088560-appb-000838
Figure PCTCN2022088560-appb-000838
(3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-二氧代哌啶-3-基)-1,3-二氧代异吲哚啉-5-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(250mg,0.23mmol)用DCM(5mL)溶解，三氟乙酸(1mL)加入，反应液室温搅拌过夜，减压浓缩，粗品使用反相制备纯化得到5-(4-((2-(1-((1S,4S)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(2,6-二氧代哌啶-3-基)异吲哚啉-1,3-二酮。(3-((1R)-1-((6-((1S,4S)-4-(4-(2-((1-(2-(2,6-dioxopiperidin-3-yl) )-1,3-dioxoisoindoline-5-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2 -Methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (250 mg, 0.23 mmol) was dissolved in DCM (5 mL), trifluoroacetic acid ( 1 mL) was added, the reaction solution was stirred at room temperature overnight, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 5-(4-((2-(1-((1S,4S)-4-(4-((((R)) -1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl )piperidin-4-yl)ethoxy)methyl)piperidin-1-carbonyl)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-di ketone.
LC-MS:(ESI,m/z):[M+H] +＝995.4. LC-MS: (ESI, m/z): [M+H] + = 995.4.
1H NMR(400MHz,DMSO-d 6)δ11.13(s,1H),8.15(s,1H),8.11(d,J＝8.1Hz,1H),8.06(s,1H),7.98(d,J＝7.6Hz,1H),7.88–7.82(m,2H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.59–5.50(m,3H),5.18(dd,J＝12.8,5.4Hz,1H),4.47-4.39(m,2H),3.95-3.85(m,4H),3.41(t,J＝6.4Hz,2H),3.24(d,J＝5.3Hz,2H),3.12-2.77(m,5H),2.70-2.55(m,4H),2.36(s,3H),2.09-1.40(m,21H),1.22-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 11.13(s, 1H), 8.15(s, 1H), 8.11(d, J=8.1Hz, 1H), 8.06(s, 1H), 7.98(d, J=7.6Hz, 1H), 7.88-7.82(m, 2H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.59-5.50(m ,3H),5.18(dd,J＝12.8,5.4Hz,1H),4.47-4.39(m,2H),3.95-3.85(m,4H),3.41(t,J＝6.4Hz,2H),3.24( d, J＝5.3Hz, 2H), 3.12-2.77(m, 5H), 2.70-2.55(m, 4H), 2.36(s, 3H), 2.09-1.40(m, 21H), 1.22-0.90(m, 4H).
实施例40：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮 Example 40: 1-(5-(4-(((1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl))) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl-2,2,6,6- d 4 )Oxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：1-苯基哌啶-2,2,6,6-d 4-4-醇的制备 Step 1: Preparation of 1-phenylpiperidin-2,2,6,6- d 4-4-ol
Figure PCTCN2022088560-appb-000839
Figure PCTCN2022088560-appb-000839
将三氟乙酸(2.34g，20.5mmol)滴入苄胺(2.19g，20.5mmol)中，加入CD 2O的D 2O溶液(20％，1.5g CD 2O溶于6mL D 2O中)，超声10分钟后，20℃搅拌1h至溶液澄清，烯丙基三甲基硅烷(2.56g,22.5mmol)加入，升温至40℃搅拌过夜，用水(10mL)稀释，用碳酸钾固体调节至pH大于9，加水(50mL)，乙酸乙酯(50mLx3)提取，饱和食盐水(100mL)洗涤有机相，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9,洗脱剂中添加1％氨水)纯化得到1-苯基哌啶-2,2,6,6-d 4-4-醇。 Trifluoroacetic acid (2.34 g, 20.5 mmol) was added dropwise to benzylamine (2.19 g, 20.5 mmol) and CD2O in D2O (20%, 1.5 g CD2O in 6 mL D2O ) was added , after sonicating for 10 minutes, stirred at 20 °C for 1 h until the solution was clear, allyltrimethylsilane (2.56 g, 22.5 mmol) was added, the temperature was raised to 40 °C, stirred overnight, diluted with water (10 mL), and adjusted to pH with potassium carbonate solid More than 9, add water (50 mL), extract with ethyl acetate (50 mL×3), wash the organic phase with saturated brine (100 mL), dry over anhydrous sodium sulfate, filter, and concentrate under reduced pressure. The crude product was subjected to column chromatography (MeOH:DCM=1: 9. Add 1% ammonia water to the eluent) and purify to obtain 1-phenylpiperidin-2,2,6,6- d 4-4-ol.
LC-MS:(ESI,m/z):[M+H] +＝196.3. LC-MS: (ESI, m/z): [M+H] + = 196.3.
步骤2：哌啶-2,2,6,6-d 4-4-醇的制备 Step 2: Preparation of piperidin-2,2,6,6- d 4-4-ol
Figure PCTCN2022088560-appb-000840
Figure PCTCN2022088560-appb-000840
将1-苯基哌啶-2,2,6,6-d 4-4-醇(470mg,2.4mmol)溶解在甲醇(30mL)中，加入Pd/C(100mg)和Pd(OH) 2/C(100mg)，氢气环境中70℃搅拌过夜，过滤，减压浓缩，得到哌啶-2,2,6,6-d 4-4-醇。 1-Phenylpiperidin-2,2,6,6-d4-4 - ol (470 mg, 2.4 mmol) was dissolved in methanol (30 mL), Pd/C (100 mg) and Pd(OH) 2 / C (100 mg), stirred overnight at 70°C under hydrogen atmosphere, filtered and concentrated under reduced pressure to give piperidin-2,2,6,6- d 4-4-ol.
LC-MS:(ESI,m/z):[M+H] +＝106.4. LC-MS: (ESI, m/z): [M+H] + = 106.4.
步骤3：4-羟基哌啶-1-羧酸-2,2,6,6-d 4叔丁酯的制备 Step 3: Preparation of 4-hydroxypiperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester
Figure PCTCN2022088560-appb-000841
Figure PCTCN2022088560-appb-000841
哌啶-2,2,6,6-d 4-4-醇(215mg,2.05mmol)用DCM(10mL)溶解，(Boc) 2O(491mg,2.26mmol)，TEA(620mg,6.15mmol)和DMAP(25mg,0.21mmol)加入，室温下搅拌过夜。反应液用水(50mL)稀释，二氯甲烷(50mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝1:1)纯化得到4-羟基哌啶-1-羧酸-2,2,6,6-d 4叔丁酯。 Piperidin-2,2,6,6-d4-4 - ol (215 mg, 2.05 mmol) was dissolved in DCM (10 mL), (Boc)2O (491 mg , 2.26 mmol), TEA (620 mg, 6.15 mmol) and DMAP (25 mg, 0.21 mmol) was added and stirred at room temperature overnight. The reaction solution was diluted with water (50 mL), extracted with dichloromethane (50 mL×3), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (EA:PE=1 : 1) Purification to obtain 4-hydroxypiperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester.
LC-MS:(ESI,m/z):[M+Na] +＝228. LC-MS: (ESI, m/z): [M+Na] + = 228.
步骤4：4-(吡啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯的制备 Step 4: Preparation of 4-(pyridin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester
Figure PCTCN2022088560-appb-000842
Figure PCTCN2022088560-appb-000842
将4-羟基哌啶-1-羧酸-2,2,6,6-d 4叔丁酯(200mg,0.98mmol)用THF(20mL)溶解，在0℃下加入NaH(60％,235mg,5.88mmol)，搅拌2小时，溴甲基吡啶氢溴酸盐(296mg,1.18mmol)加入，反应液加热到70℃搅拌过夜。用水(50mL)稀释，乙酸乙酯(50mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:19)纯化得到4-(吡啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯。 4-Hydroxypiperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester (200 mg, 0.98 mmol) was dissolved in THF (20 mL), NaH (60%, 235 mg, 5.88 mmol), stirred for 2 hours, bromomethylpyridine hydrobromide (296 mg, 1.18 mmol) was added, and the reaction solution was heated to 70 °C and stirred overnight. It was diluted with water (50 mL), extracted with ethyl acetate (50 mL×3), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was subjected to column chromatography (MeOH:DCM=1:19). ) was purified to give 4-(pyridin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝297.2. LC-MS: (ESI, m/z): [M+H] + = 297.2.
步骤5：4-(哌啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯的制备 Step 5: Preparation of 4-(piperidin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester
Figure PCTCN2022088560-appb-000843
Figure PCTCN2022088560-appb-000843
将4-(吡啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯(150mg，0.51mmol)用异丙醇(6mL)和水(7mL)的混合溶液溶解，Pd(OH) 2/C(45mg)加入，氢气环境中70℃搅拌过夜。过滤，减压浓缩，得到4-(哌啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯。 4-(Pyridin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester (150 mg, 0.51 mmol) was dissolved in isopropanol (6 mL) and water ( 7 mL) of the mixed solution was dissolved, Pd(OH) 2 /C (45 mg) was added, and the mixture was stirred at 70° C. overnight in a hydrogen atmosphere. Filtration and concentration under reduced pressure gave 4-(piperidin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝303.2. LC-MS: (ESI, m/z): [M+H] + = 303.2.
步骤6：4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯的制备 Step 6: 4-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy) Preparation of piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester
Figure PCTCN2022088560-appb-000844
Figure PCTCN2022088560-appb-000844
将4-(哌啶-4-基甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯(130mg,0.43mmol)用DMSO(5mL)溶解，加入DIEA(133mg,1.04mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)benzoate苯甲酸五氟苯酯(150mg,0.35mmol)，反应液室温搅拌2h，加水(30mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯。 4-(Piperidin-4-ylmethoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester (130 mg, 0.43 mmol) was dissolved in DMSO (5 mL) and DIEA was added (133mg, 1.04mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate pentafluorophenyl benzoate (150mg, 0.35mmol), the reaction solution was stirred at room temperature For 2 h, add water (30 mL) and stir for 5 minutes, extract with ethyl acetate (30 mL×3), wash the organic phase with saturated brine (50 mL), dry over anhydrous sodium sulfate, filter, concentrate under reduced pressure, and the crude product is subjected to column chromatography (MeOH). : DCM=1:9) to give 4-((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidine-4- yl)methoxy)piperidine-1-carboxylic acid-2,2,6,6-d 4 -tert-butyl ester.
LC-MS:(ESI,m/z):[M+Na] +＝575.3. LC-MS: (ESI, m/z): [M+Na] + = 575.3.
步骤7：1-(2-氯-5-(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 7: 1-(2-Chloro-5-(4-(((piperidin-4-yl-2,2,6,6- d4 )oxy)methyl)piperidine-1-carbonyl)phenyl ) Preparation of dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000845
Figure PCTCN2022088560-appb-000845
将4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羧酸-2,2,6,6-d 4叔丁酯(130mg,0.24mmol)用DCM(5mL)溶解，三氟乙酸(1mL)加入，室温搅拌2小时，减压浓缩得到1-(2-氯-5-(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，直接用于下一步。 4-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)piperidine -1-Carboxylic acid-2,2,6,6-d 4 -tert-butyl ester (130 mg, 0.24 mmol) was dissolved in DCM (5 mL), trifluoroacetic acid (1 mL) was added, stirred at room temperature for 2 hours, and concentrated under reduced pressure to obtain 1 -(2-Chloro-5-(4-(((piperidin-4-yl-2,2,6,6-d 4 )oxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine -2,4(1H,3H)-dione, used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝453.2. LC-MS: (ESI, m/z): [M+H] + = 453.2.
步骤8：(3-((R)-1-((6-((1R,4R)-4-(4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备 Step 8: (3-((R)-1-((6-((1R,4R)-4-(4-((1-(4-Chloro-3-(2,4-dioxotetrahydro) Pyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)piperidine-1-carbonyl-2,2,6,6-d 4 )cyclohexyl)-7-methoxy Preparation of tert-butyl-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000846
Figure PCTCN2022088560-appb-000846
将1-(2-氯-5-(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(130mg,0.29mmol)用DMSO(5mL)溶解，加入(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(130mg,0.22mmol)，HATU(110mg,0.29mmol)和DIEA(142mg,1.10mmol)，室温搅拌2小时，加水(30mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。 1-(2-Chloro-5-(4-(((piperidin-4-yl-2,2,6,6-d 4 )oxy)methyl)piperidine-1-carbonyl)phenyl)di Hydropyrimidine-2,4(1H,3H)-dione (130 mg, 0.29 mmol) was dissolved in DMSO (5 mL), (1R,4R)-4-(4-(((R)-1-(3- ((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 - Carboxylic acid (130 mg, 0.22 mmol), HATU (110 mg, 0.29 mmol) and DIEA (142 mg, 1.10 mmol), stirred at room temperature for 2 hours, added water (30 mL) and stirred for 5 minutes, extracted with ethyl acetate (30 mL x 3), saturated The organic phase was washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (MeOH:DCM=1:9) to give (3-((R)-1-(( 6-((1R,4R)-4-(4-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidine -4-yl)methoxy)piperidine-1-carbonyl-2,2,6,6- d4 )cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino ) ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1037.5. LC-MS: (ESI, m/z): [M+H] + = 1037.5.
步骤9：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 9: 1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl-2,2,6,6-d 4 ) Preparation of oxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000847
Figure PCTCN2022088560-appb-000847
将(3-((R)-1-((6-((1R,4R)-4-(4-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(130mg,0.13mmol)溶于DCM(5mL)，TFA(1mL)加入，室温搅拌2小时，减压浓缩，粗品用DCM(20mL)溶解，用饱和碳酸氢钠水溶液(20mL)调节pH至中性，搅拌10分钟，用MeOH/DCM(v:v＝1:9,20mL×3)提取，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine- 1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)piperidine-1-carbonyl-2,2,6,6- d4 )cyclohexyl)-7-methoxy- 2-Methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (130 mg, 0.13 mmol) was dissolved in DCM (5 mL), TFA (1 mL) ) was added, stirred at room temperature for 2 hours, concentrated under reduced pressure, the crude product was dissolved in DCM (20 mL), adjusted to neutral pH with saturated aqueous sodium bicarbonate solution (20 mL), stirred for 10 minutes, and then mixed with MeOH/DCM (v:v=1: 9, 20mL×3), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(4-(((1-((1R,4R)-4- (4-(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl )cyclohexane-1-carbonyl)piperidin-4-yl-2,2,6,6-d 4 )oxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine- 2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝937.4. LC-MS: (ESI, m/z): [M+H] + = 937.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.14-8.02(m,2H),7.64(d,J＝8.2Hz,1H),7.54(d,J＝1.9Hz,1H),7.38(dd,J＝8.2,1.9Hz,1H),6.99(s,1H),6.86(d,J＝10.5Hz,2H),6.70(s,1H),5.64-5.46(m,3H),4.51-4.39(m,1H),3.88(s,3H),3.75-3.42(m,4H),3.12–3.01(m,1H),2.95(t,J＝11.2Hz,1H),2.83–2.57(m,5H),2.35(s,3H),1.95-1.50(m,17H),1.45-1.27(m,2H),1.25-1.07(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 8.14-8.02(m, 2H), 7.64(d, J=8.2Hz, 1H), 7.54(d, J=1.9Hz, 1H), 7.38(dd, J=8.2, 1.9Hz, 1H), 6.99(s, 1H), 6.86(d, J=10.5Hz, 2H), 6.70(s, 1H), 5.64-5.46(m, 3H) ), 4.51-4.39(m, 1H), 3.88(s, 3H), 3.75-3.42(m, 4H), 3.12-3.01(m, 1H), 2.95(t, J＝11.2Hz, 1H), 2.83- 2.57(m, 5H), 2.35(s, 3H), 1.95-1.50(m, 17H), 1.45-1.27(m, 2H), 1.25-1.07(m, 2H).
实施例41：5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-基)-2-(2,4-二氧代环己基)异吲哚啉-1,3-二酮Example 41: 5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) Amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine-4 -yl)ethoxy)methyl)piperidin-1-yl)-2-(2,4-dioxocyclohexyl)isoindoline-1,3-dione
步骤1：4-(2-((1-(2-(2,4-二氧代环己基)-1,3-二氧代异吲哚啉-5-基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(2-((1-(2-(2,4-dioxocyclohexyl)-1,3-dioxoisoindolin-5-yl)piperidin-4-yl) Preparation of tert-butyl methoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000848
Figure PCTCN2022088560-appb-000848
向4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(430mg,1.3mmol)和2-(2,6-二氧代哌啶-3-基)-5-氟异吲哚啉-1,3-二酮(718mg,2.6mmol)的DMF(3mL)溶液中加入DIEA(675mg,3.9mmol)，反应混合物加热到110℃并搅拌过夜。反应液倒入水中，用EA(30ml×2)，有机相用无水Na 2SO 4干燥，减压浓缩，所得粗品经自动过主机(EA/PE)纯化得到4-(2-((1-(2-(2,4-二氧代环己基)-1,3-二氧代异吲哚啉-5-基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。 To 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (430 mg, 1.3 mmol) and 2-(2,6-dioxopiperidine- 3-yl)-5-fluoroisoindoline-1,3-dione (718 mg, 2.6 mmol) in DMF (3 mL) was added DIEA (675 mg, 3.9 mmol) and the reaction mixture was heated to 110 °C and stirred overnight . The reaction solution was poured into water, EA (30ml×2) was used, the organic phase was dried with anhydrous Na 2 SO 4 and concentrated under reduced pressure. The obtained crude product was automatically purified by main engine (EA/PE) to obtain 4-(2-((1 -(2-(2,4-Dioxocyclohexyl)-1,3-dioxoisoindolin-5-yl)piperidin-4-yl)methoxy)ethyl)piperidine-1 - tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝583.4. LC-MS: (ESI, m/z): [M+H] + = 583.4.
步骤2：2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)异吲哚啉-1,3-二酮的制备Step 2: 2-(2,6-Dioxopiperidin-3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidin-1- Preparation of Isoindoline-1,3-dione
Figure PCTCN2022088560-appb-000849
Figure PCTCN2022088560-appb-000849
将4-(2-((1-(2-(2,4-二氧代环己基)-1,3-二氧代异吲哚啉-5-基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯(210mg,0.36mmol)的HCI/1,4-二氧六环(4M,5mL)溶液在室温搅拌1h。反应液直接浓缩得到2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)异吲哚啉-1,3-二酮。4-(2-((1-(2-(2,4-dioxocyclohexyl)-1,3-dioxoisoindolin-5-yl)piperidin-4-yl)methoxy A solution of tert-butyl)ethyl)piperidine-1-carboxylate (210 mg, 0.36 mmol) in HCl/1,4-dioxane (4M, 5 mL) was stirred at room temperature for 1 h. The reaction solution was directly concentrated to obtain 2-(2,6-dioxopiperidin-3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine- 1-yl)isoindoline-1,3-dione.
LC-MS:(ESI,m/z):[M+H] +＝483.3. LC-MS: (ESI, m/z): [M+H] + = 483.3.
步骤3：5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-基)-2-(2,4-二氧代环己基)异吲哚啉-1,3-二酮的制备Step 3: 5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethylamino) )methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine-4- Preparation of yl)ethoxy)methyl)piperidin-1-yl)-2-(2,4-dioxocyclohexyl)isoindoline-1,3-dione
Figure PCTCN2022088560-appb-000850
Figure PCTCN2022088560-appb-000850
向(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(100mg,0.17mmol和2-(2,6-二氧代哌啶-3-基)-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)异吲哚啉-1,3-二酮(87mg,0.17mmol)的DMF(5mL)溶液中加入HATU(77mg,0.20mmol)和DIEA(65mg,0.51mmol)。反应液在室温搅拌2h。反应液倒入水中，并用EA(20mL×3)萃取，无水Na 2SO 4干燥，减压浓缩，所得粗品经prep-HPLC纯化得到5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-基)-2-(2,4-二氧代环己基)异吲哚啉-1,3-二酮。 To (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (100 mg, 0.17 mmol and 2-(2,6-dioxopiperidine- 3-yl)-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidin-1-yl)isoindoline-1,3-dione (87mg, 0.17 mmol) in DMF (5 mL) solution was added HATU (77 mg, 0.20 mmol) and DIEA (65 mg, 0.51 mmol). The reaction solution was stirred at room temperature for 2 h. The reaction solution was poured into water and extracted with EA (20 mL×3). It was dried over Na 2 SO 4 and concentrated under reduced pressure, and the resulting crude product was purified by prep-HPLC to give 5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1) -(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6 -yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidin-1-yl)-2-(2,4-dioxocyclohexyl)isoindoline -1,3-Dione.
LC-MS:(ESI,m/z):[M-H] -＝1057.4. LC-MS: (ESI, m/z): [MH] - = 1057.4.
1H NMR(400MHz,DMSO-d 6)δ11.07(s,1H),8.31(d,J＝8.1Hz,1H),8.05(s,1H),7.64(d,J＝8.5Hz,1H),7.49–7.38(m,2H),7.36–7.29(m,2H),7.23(dd,J＝9.8,1.7Hz,2H),7.02(s,1H),6.96(s,1H),6.03–5.87(m,1H),5.10-5.00(m,1H),4.42-4.31(m,1H),4.10-4.00(m,2H),3.97-3.85(m,4H),3.41(t,J＝6.3Hz,2H),3.23(d,J＝6.2Hz,2H),3.18–3.07(m,2H),3.05–2.81(m,5H),2.71–2.52(m,3H),2.42(s,3H),2.01(s,6H),1.89- 1.44(m,20H),1.26-0.86(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 11.07 (s, 1H), 8.31 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.64 (d, J=8.5 Hz, 1H) ,7.49–7.38(m,2H),7.36–7.29(m,2H),7.23(dd,J=9.8,1.7Hz,2H),7.02(s,1H),6.96(s,1H),6.03–5.87 (m,1H),5.10-5.00(m,1H),4.42-4.31(m,1H),4.10-4.00(m,2H),3.97-3.85(m,4H),3.41(t,J=6.3Hz ,2H),3.23(d,J＝6.2Hz,2H),3.18-3.07(m,2H),3.05-2.81(m,5H),2.71-2.52(m,3H),2.42(s,3H), 2.01(s,6H),1.89- 1.44(m,20H),1.26-0.86(m,4H).
实施例42：(R)-1-(5-(9-(((3-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 42: (R)-1-(5-(9-(((3-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)) Amino)-2,7-Dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)amino)methyl)-3-azaspiro [5.5]Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(3-羟基丙基)(甲基)羧酸苄酯的制备Step 1: Preparation of benzyl (3-hydroxypropyl)(methyl)carboxylate
Figure PCTCN2022088560-appb-000851
Figure PCTCN2022088560-appb-000851
将3-(甲基氨基)丙烷-1-醇(5.0g,56.17mmol)和氯甲酸苄酯(10.5g,61.79mmol)溶于1,4-二氧六环(40mL)中，再加入氢氧化钠溶液(2mol/L,48mL)在50℃下搅拌0.5小时，直接减压浓缩得到粗品(3-羟基丙基)(甲基)羧酸苄酯。3-(Methylamino)propan-1-ol (5.0 g, 56.17 mmol) and benzyl chloroformate (10.5 g, 61.79 mmol) were dissolved in 1,4-dioxane (40 mL) and hydrogen was added The sodium oxide solution (2 mol/L, 48 mL) was stirred at 50° C. for 0.5 hours, and then directly concentrated under reduced pressure to obtain the crude benzyl (3-hydroxypropyl)(methyl)carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝224.3. LC-MS: (ESI, m/z): [M+H] + = 224.3.
步骤2：(3-溴丙基)(甲基)羧酸苄酯的制备Step 2: Preparation of benzyl (3-bromopropyl)(methyl)carboxylate
Figure PCTCN2022088560-appb-000852
Figure PCTCN2022088560-appb-000852
将(3-羟基丙基)(甲基)羧酸苄酯(4.6g,20mmol)溶于四氢呋喃(40mL)，三苯基磷(7.8g,30mmol)和四溴化碳(10g,30mmol)分别加入，反应液室温下搅拌2小时，用水(200mL)稀释，乙酸乙酯(200mL×3)萃取，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝1:1)纯化得到(3-溴丙基)(甲基)羧酸苄酯。Benzyl (3-hydroxypropyl)(methyl)carboxylate (4.6g, 20mmol) was dissolved in tetrahydrofuran (40mL), triphenylphosphine (7.8g, 30mmol) and carbon tetrabromide (10g, 30mmol) were respectively was added, the reaction solution was stirred at room temperature for 2 hours, diluted with water (200 mL), extracted with ethyl acetate (200 mL×3), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was subjected to column chromatography (PE:EA=1:1) Purification gave benzyl (3-bromopropyl)(methyl)carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝288.1. LC-MS: (ESI, m/z): [M+H] + = 288.1.
步骤3：(3-(4-溴-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯的制备Step 3: Preparation of benzyl (3-(4-bromo-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate
Figure PCTCN2022088560-appb-000853
Figure PCTCN2022088560-appb-000853
将4-溴吡啶-2(1H)-酮(790mg,4.5mmol)用无水DMF(5mL)溶解并降至0℃，NaH(218mg,5.5mmol)加入，反应液搅拌0.5小时，然后在室温下加入(3-溴丙基)(甲基)羧酸苄酯(1.3g,4.5mmol)并搅拌12小时，用水(100mL)稀释，乙酸乙酯(150mL×4)萃取，有机相用饱和食盐水洗(100mL)，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(PE:EA＝1:2)纯化得到(3-(4-溴-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯。4-Bromopyridin-2(1H)-one (790 mg, 4.5 mmol) was dissolved in anhydrous DMF (5 mL) and lowered to 0 °C, NaH (218 mg, 5.5 mmol) was added, the reaction solution was stirred for 0.5 hours, and then at room temperature Benzyl (3-bromopropyl)(methyl)carboxylate (1.3 g, 4.5 mmol) was added and stirred for 12 hours, diluted with water (100 mL), extracted with ethyl acetate (150 mL×4), and the organic phase was saturated with common salt Washed with water (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was purified by column chromatography (PE:EA=1:2) to obtain (3-(4-bromo-2-oxopyridine-1(2H) )-yl)propyl)(methyl)carboxylate benzyl ester.
LC-MS:(ESI,m/z):(ESI,m/z):[M+H] +＝379.0. LC-MS: (ESI, m/z): (ESI, m/z): [M+H] + =379.0.
步骤4：甲基(3-(2-氧代-4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)吡啶-1(2H)-基)丙基)羧酸苄酯的制备Step 4: Methyl(3-(2-oxo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)pyridine-1(2H )-yl)propyl) benzyl carboxylate preparation
Figure PCTCN2022088560-appb-000854
Figure PCTCN2022088560-appb-000854
将(3-(4-溴-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯(1.2g，3.2mmol)和4,4,4',4',5,5,5',5'-八甲基-2,2'-二(1,3,2-二氧硼戊烷)(979mg，3.8mmol)用无水1,4-二氧六环溶解，加入Pd(dppf)Cl 2(120mg)和碳酸钾(880mg,6.47mmol)然后在氮气保护下100℃搅拌过夜，用水(100mL)稀释，乙酸乙酯(100mL×3)萃取，有机相用饱和食盐水洗(100mL)，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(乙酸乙酯：石油醚＝1:1)纯化得到产品甲基(3-(2-氧代-4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)吡啶-1(2H)-基)丙基)羧酸苄酯。 Benzyl (3-(4-bromo-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate (1.2 g, 3.2 mmol) and 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bis(1,3,2-dioxaboropentane) (979mg, 3.8mmol) was treated with anhydrous 1,4-dioxane The ring was dissolved, Pd(dppf)Cl 2 (120 mg) and potassium carbonate (880 mg, 6.47 mmol) were added, then stirred at 100 °C overnight under nitrogen protection, diluted with water (100 mL), extracted with ethyl acetate (100 mL×3), and the organic phase was Washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (ethyl acetate:petroleum ether=1:1) to obtain the product methyl (3-(2-oxo) - Benzyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)pyridin-1(2H)-yl)propyl)carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝427.4. LC-MS: (ESI, m/z): [M+H] + = 427.4.
步骤5：(3-(4-(4-羟基-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯的制备Step 5: (3-(4-(4-Hydroxy-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl) Preparation of benzyl carboxylate
Figure PCTCN2022088560-appb-000855
Figure PCTCN2022088560-appb-000855
将6-溴-2,7-二甲基喹唑啉-4-醇(450mg,1.77mmol)和甲基(3-(2-氧代-4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)吡啶-1(2H)-基)丙基)羧酸苄酯(980mg,2.3mmol)溶于DMF/水溶液中(10/1,4mL)中，加入碳酸钾(480mg,3.5mmol)和Pd(dppf)Cl 2(90mg)，氮气置换，在氮气保护下加热到100℃搅拌2小时，用水(50mL)稀释，乙酸乙酯(50mL×3)萃取,有机相用饱和食盐水洗(100mL)，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(DCM:MEOH＝10:1)纯化得到产品(3-(4-(4-羟基-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯。 6-Bromo-2,7-dimethylquinazolin-4-ol (450 mg, 1.77 mmol) and methyl (3-(2-oxo-4-(4,4,5,5-tetramethyl) Benzyl-1,3,2-dioxaboropentan-2-yl)pyridin-1(2H)-yl)propyl)carboxylate (980 mg, 2.3 mmol) was dissolved in DMF/water solution (10/1 , 4 mL), potassium carbonate (480 mg, 3.5 mmol) and Pd(dppf)Cl 2 (90 mg) were added, replaced with nitrogen, heated to 100 °C under nitrogen, stirred for 2 hours, diluted with water (50 mL), ethyl acetate ( 50mL×3) extraction, the organic phase was washed with saturated brine (100mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (DCM:MEOH=10:1) to obtain the product (3-(4). -(4-Hydroxy-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate benzyl ester.
LC-MS:(ESI,m/z):(ESI,m/z):[M+H] +＝473.3. LC-MS: (ESI, m/z): (ESI, m/z): [M+H] + = 473.3.
步骤6：(R)-(3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯的制备Step 6: (R)-(3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- Preparation of benzyl 2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate
Figure PCTCN2022088560-appb-000856
Figure PCTCN2022088560-appb-000856
将(3-(4-(4-羟基-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯(480mg,1.02mmol)用DMF(4mL)溶解，加入DBU(388mg,2.55mmol)和BOP(583mg,1.32mmol)，在室温下搅拌0.5小时，加入(R)-(3-(1-氨乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(403mg,1.32mmol)，反应液加热到70℃搅拌过夜，加水(50mL)稀释，乙酸乙酯(50mL×3)萃取，有机相用饱和食盐水(100mL)洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(乙酸乙酯:石油醚＝1:1)纯化得到产品(R)-(3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯。(3-(4-(4-Hydroxy-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylic acid Benzyl ester (480 mg, 1.02 mmol) was dissolved in DMF (4 mL), DBU (388 mg, 2.55 mmol) and BOP (583 mg, 1.32 mmol) were added, and the mixture was stirred at room temperature for 0.5 h. (R)-(3-(1- Aminoethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (403 mg, 1.32 mmol), the reaction solution was heated to 70 °C and stirred overnight, diluted with water (50 mL), ethyl acetate (50 mL×3 ) extraction, the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (ethyl acetate:petroleum ether=1:1) to obtain the product (R)- (3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethyl Quinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝759.4. LC-MS: (ESI, m/z): [M+H] + =759.4.
步骤7：(R)-(3-(1-((2,7-二甲基-6-(1-(3-(甲基氨基)丙基)-2-氧代-1,2-二氢吡啶-4-基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 7: (R)-(3-(1-((2,7-Dimethyl-6-(1-(3-(methylamino)propyl)-2-oxo-1,2-di) Preparation of tert-butyl hydropyridin-4-yl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000857
Figure PCTCN2022088560-appb-000857
将(R)-(3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)羧酸苄酯(300mg,0.4mmol)用乙酸乙酯(4mL)溶解，Pd/C(60mg)加入，置换氢气，在氢气氛围下室温搅拌2小时，过滤浓缩得到粗品(R)-(3-(1-((2,7-二甲基-6-(1-(3-(甲基氨基)丙基)-2-氧代-1,2-二氢吡啶-4-基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。(R)-(3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-2, Benzyl 7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)carboxylate (300 mg, 0.4 mmol) was treated with ethyl acetate (4 mL) ) was dissolved, Pd/C (60 mg) was added, hydrogen was replaced, stirred at room temperature for 2 hours under a hydrogen atmosphere, filtered and concentrated to obtain crude product (R)-(3-(1-((2,7-dimethyl-6-( 1-(3-(Methylamino)propyl)-2-oxo-1,2-dihydropyridin-4-yl)quinazolin-4-yl)amino)ethyl)-5-(trifluoro Methyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝625.5. LC-MS: (ESI, m/z): [M+H] + = 625.5.
步骤8：(R)-9-(((3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 8: (R)-9-(((3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl )amino)-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)methyl)amino)methyl)-3-azaspiro Preparation of [5.5] Undecane-3-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000858
Figure PCTCN2022088560-appb-000858
将(R)-(3-(1-((2,7-二甲基-6-(1-(3-(甲基氨基)丙基)-2-氧代-1,2-二氢吡啶-4-基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(130mg，0.21mmol)和9-醛基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(59mg,0.21mmol)用THF(4mL)溶解，三乙酰氧基硼氢化钠(131mg,0.63mmol)加入，在室温下搅拌2小时，用水(50mL)稀释，乙酸乙酯(30mL×3)萃取，有机相用饱和食盐水(50mL)洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(二氯甲烷:甲醇＝10:1)纯化得到产品(R)-9-(((3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。(R)-(3-(1-((2,7-Dimethyl-6-(1-(3-(methylamino)propyl)-2-oxo-1,2-dihydropyridine) -4-yl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (130 mg, 0.21 mmol) and 9-aldehyde-3-nitrogen Heteraspiro[5.5]undecane-3-carboxylate tert-butyl ester (59 mg, 0.21 mmol) was dissolved in THF (4 mL), sodium triacetoxyborohydride (131 mg, 0.63 mmol) was added, and the mixture was stirred at room temperature for 2 hours , diluted with water (50 mL), extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (dichloromethane: Methanol=10:1) to obtain the product (R)-9-(((3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) )phenyl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)methyl)amino)methyl) - tert-butyl 3-azaspiro[5.5]undecane-3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝890.5. LC-MS: (ESI, m/z): [M+H] + = 890.5.
步骤9：(R)-1-(3-(((3-氮杂螺[5.5]十一烷-9-基)甲基)(甲基)氨基)丙基)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)吡啶-2(1H)-酮的制备Step 9: (R)-1-(3-(((3-Azaspiro[5.5]undecan-9-yl)methyl)(methyl)amino)propyl)-4-(4-( Preparation of (1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)pyridin-2(1H)-one
Figure PCTCN2022088560-appb-000859
Figure PCTCN2022088560-appb-000859
将(R)-9-(((3-(4-(4-((1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(100mg,0.11mmol)，加入到氯化氢的1,4-二氧六环溶液(4M,3mL)在室温下反应2小时，直接减压浓缩得到粗产品(R)-1-(3-(((3-氮杂螺[5.5]十一烷-9-基)甲基)(甲基)氨基)丙基)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)吡啶-2(1H)-酮。(R)-9-(((3-(4-(4-((1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino )-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)methyl)amino)methyl)-3-azaspiro[5.5 ] Undecane-3-carboxylate tert-butyl ester (100 mg, 0.11 mmol) was added to a solution of hydrogen chloride in 1,4-dioxane (4 M, 3 mL) to react at room temperature for 2 hours, and then directly concentrated under reduced pressure to obtain crude Product (R)-1-(3-(((3-Azaspiro[5.5]undecan-9-yl)methyl)(methyl)amino)propyl)-4-(4-((1 -(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)pyridin-2(1H)-one.
LC-MS:(ESI,m/z):[M+H] +＝690.5. LC-MS: (ESI, m/z): [M+H] + = 690.5.
步骤10：(R)-1-(5-(9-(((3-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 10: (R)-1-(5-(9-(((3-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino )-2,7-Dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)amino)methyl)-3-azaspiro[ 5.5] Preparation of Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000860
Figure PCTCN2022088560-appb-000860
将(R)-1-(3-(((3-氮杂螺[5.5]十一烷-9-基)甲基)(甲基)氨基)丙基)-4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)吡啶-2(1H)-酮(80mg,0.12mmol)和perfluorophenyl 4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(51mg,0.12mmol)溶于DMSO(3mL)，DIEA(60mg,0.48mmol)加入，反应液室温下搅拌2小时，用水(30mL)稀释，乙酸乙酯(30mL*3)萃取，饱和食盐水洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用Prep-HPLC纯化得到产品(R)-1-(5-(9-(((3-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)-2-氧代吡啶-1(2H)-基)丙基)(甲基)氨基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(R)-1-(3-(((3-Azaspiro[5.5]undecan-9-yl)methyl)(methyl)amino)propyl)-4-(4-(((1 -(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)pyridin-2(1H)-one (80 mg, 0.12 mmol) and perfluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (51 mg, 0.12 mmol) in DMSO (3 mL), DIEA ( 60 mg, 0.48 mmol) was added, the reaction solution was stirred at room temperature for 2 hours, diluted with water (30 mL), extracted with ethyl acetate (30 mL*3), washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was used Prep-HPLC purification gave the product (R)-1-(5-(9-(((3-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) yl)amino)-2,7-dimethylquinazolin-6-yl)-2-oxopyridin-1(2H)-yl)propyl)(methyl)amino)methyl)-3-nitrogen Heterospiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M-H] -＝940.5. LC-MS: (ESI, m/z): [MH] - = 940.5.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.36(d,J＝8.2Hz,1H),8.29(s,1H),7.73(d,J＝6.6Hz,1H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.50(s,1H),7.38(d,J＝8.3Hz,1H),6.88(s,1H),6.84(s,1H),6.69(s,1H),6.42(s,1H),6.36(d,J＝7.0Hz,1H),5.60-5.48(m,3H),4.00-3.90(m,2H),3.80-3.50(m,5H),3.29-3.20(m,3H),2.77-2.70(m,2H),2.44-2.26(m,7H),2.20-2.06(m,4H),1.87-1.78(m,2H),1.74-1.65(m,2H),1.62-1.20(m,10H),1.16-0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.36(d, J=8.2Hz, 1H), 8.29(s, 1H), 7.73(d, J=6.6Hz, 1H) ,7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.50(s,1H),7.38(d,J＝8.3Hz,1H),6.88(s,1H),6.84(s, 1H), 6.69(s, 1H), 6.42(s, 1H), 6.36(d, J=7.0Hz, 1H), 5.60-5.48(m, 3H), 4.00-3.90(m, 2H), 3.80-3.50 (m,5H),3.29-3.20(m,3H),2.77-2.70(m,2H),2.44-2.26(m,7H),2.20-2.06(m,4H),1.87-1.78(m,2H) ,1.74-1.65(m,2H),1.62-1.20(m,10H),1.16-0.92(m,4H).
实施例43：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)- 2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 43: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl )-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-甲氧基乙氧基)-2-硝基苯甲酸甲酯的制备Step 1: Preparation of methyl 4-(2-methoxyethoxy)-2-nitrobenzoate
Figure PCTCN2022088560-appb-000861
Figure PCTCN2022088560-appb-000861
在三口瓶中加入2-甲氧基乙烷-1-醇(365mg,4.8mmol)，用THF(10mL)溶解，置换三次氮气，在0℃条件下加入t-BuOK(1M/THF,4.2mL,4.2mmol)，0℃反应1h后滴加4-氟-2-硝基苯甲酸甲酯(600mg,3.0mmol)的THF(10mL)溶液，继续在0℃反应2h后，加水(50mL)，用乙酸乙酯(50mLx3)萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝2:3)纯化得到4-(2-甲氧基乙氧基)-2-硝基苯甲酸甲酯。2-Methoxyethane-1-ol (365 mg, 4.8 mmol) was added to a three-necked flask, dissolved in THF (10 mL), nitrogen was replaced three times, and t-BuOK (1M/THF, 4.2 mL) was added at 0°C , 4.2 mmol), reacted at 0 °C for 1 h and added dropwise a solution of methyl 4-fluoro-2-nitrobenzoate (600 mg, 3.0 mmol) in THF (10 mL), continued to react at 0 °C for 2 h, and added water (50 mL), Extracted with ethyl acetate (50 mL×3), washed the organic phase with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (EA:PE=2:3) to obtain 4- (2-Methoxyethoxy)-2-nitrobenzoic acid methyl ester.
1H NMR(400MHz,DMSO-d 6)δ7.87(d,J＝8.7Hz,1H),7.57(d,J＝2.5Hz,1H),7.34(dd,J＝8.7,2.5Hz,1H),4.29–4.24(m,2H),3.81(s,3H),3.70–3.66(m,2H),3.31(s,3H). 1 H NMR (400MHz, DMSO-d 6 ) δ 7.87 (d, J=8.7Hz, 1H), 7.57 (d, J=2.5Hz, 1H), 7.34 (dd, J=8.7, 2.5Hz, 1H) ,4.29–4.24(m,2H),3.81(s,3H),3.70–3.66(m,2H),3.31(s,3H).
步骤2：2-氨基-4-(2-甲氧基乙氧基)苯甲酸甲酯的制备Step 2: Preparation of methyl 2-amino-4-(2-methoxyethoxy)benzoate
Figure PCTCN2022088560-appb-000862
Figure PCTCN2022088560-appb-000862
将4-(2-甲氧基乙氧基)-2-硝基苯甲酸甲酯(850mg,3.3mmol)，溶于EtOH(20mL)，加入Raney-Ni(1mL)，在H 2氛围中室温搅拌2h，过滤，减压浓缩，得到2-氨基-4-(2-甲氧基乙氧基)苯甲酸甲酯。 Methyl 4-(2-methoxyethoxy)-2-nitrobenzoate (850 mg, 3.3 mmol) was dissolved in EtOH (20 mL), Raney-Ni ( 1 mL) was added, and room temperature under H atmosphere Stir for 2 h, filter, and concentrate under reduced pressure to obtain methyl 2-amino-4-(2-methoxyethoxy)benzoate.
LC-MS:(ESI,m/z):[M+H] +＝226.1. LC-MS: (ESI, m/z): [M+H] + = 226.1.
步骤3：2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸甲酯的制备Step 3: Preparation of methyl 2-amino-5-bromo-4-(2-methoxyethoxy)benzoate
Figure PCTCN2022088560-appb-000863
Figure PCTCN2022088560-appb-000863
将2-氨基-4-(2-甲氧基乙氧基)苯甲酸甲酯(680mg,3.0mmol)用DMF(10mL)溶解，0℃加入NBS(484mg,2.7mmol)，0℃反应1h，加水(100mL)并搅拌5分钟，用乙酸乙酯(100mLx3)萃取，饱和食盐水(200mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(EA:PE＝2:3)纯化得到2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸甲酯。Methyl 2-amino-4-(2-methoxyethoxy)benzoate (680 mg, 3.0 mmol) was dissolved in DMF (10 mL), NBS (484 mg, 2.7 mmol) was added at 0 °C, and the reaction was carried out at 0 °C for 1 h, Water (100 mL) was added and stirred for 5 minutes, extracted with ethyl acetate (100 mL×3), the organic phase was washed with saturated brine (200 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (EA:PE =2:3) Purification to obtain methyl 2-amino-5-bromo-4-(2-methoxyethoxy)benzoate.
LC-MS:(ESI,m/z):[M+H] +＝304.0. LC-MS: (ESI, m/z): [M+H] + = 304.0.
步骤4：2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸的制备Step 4: Preparation of 2-amino-5-bromo-4-(2-methoxyethoxy)benzoic acid
Figure PCTCN2022088560-appb-000864
Figure PCTCN2022088560-appb-000864
将2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸甲酯(710mg,2.3mmol)溶于THF/H 2O(15mL,2:1)中，加入LiOH(570mg,23.0mmol)，50℃搅拌过夜，加水(20mL)，用1M盐酸调节pH至6，用MeOH/DCM混合溶液(1/10,30mLx3)萃取，经无水硫酸钠干燥，过滤，减压浓缩，得到2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸。 Methyl 2-amino-5-bromo-4-(2-methoxyethoxy)benzoate (710 mg, 2.3 mmol) was dissolved in THF/H 2 O (15 mL, 2:1) and LiOH ( 570 mg, 23.0 mmol), stirred at 50 °C overnight, added water (20 mL), adjusted pH to 6 with 1 M hydrochloric acid, extracted with a mixed solution of MeOH/DCM (1/10, 30 mL×3), dried over anhydrous sodium sulfate, filtered, and reduced pressure Concentration gave 2-amino-5-bromo-4-(2-methoxyethoxy)benzoic acid.
LC-MS:(ESI,m/z):[M+3] +＝292.0. LC-MS: (ESI, m/z): [M+3] + = 292.0.
步骤5：6-溴-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-醇的制备Step 5: Preparation of 6-bromo-7-(2-methoxyethoxy)-2-methylquinazolin-4-ol
Figure PCTCN2022088560-appb-000865
Figure PCTCN2022088560-appb-000865
在闷罐中加入2-氨基-5-溴-4-(2-甲氧基乙氧基)苯甲酸(665mg,2.3mmol)，用MeOH(20mL)溶解，加入乙酸铵(2.66g,34.5mmol)和原乙酸三甲酯(4.14g,34.5mmol)，120℃反应过夜，减压浓缩除去甲醇，加水(50mL)，用乙酸乙酯(50mLx3)萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:4)纯化得到6-溴-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-醇。2-Amino-5-bromo-4-(2-methoxyethoxy)benzoic acid (665 mg, 2.3 mmol) was added to a stuffy pot, dissolved in MeOH (20 mL), and ammonium acetate (2.66 g, 34.5 mmol) was added. ) and trimethyl orthoacetate (4.14g, 34.5mmol), reacted at 120°C overnight, concentrated under reduced pressure to remove methanol, added water (50mL), extracted with ethyl acetate (50mL×3), washed the organic phase with saturated brine (100mL), It was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (MeOH:DCM=1:4) to give 6-bromo-7-(2-methoxyethoxy)-2-methyl Quinazolin-4-ol.
LC-MS:(ESI,m/z):[M+H] +＝312.9. LC-MS: (ESI, m/z): [M+H] + = 312.9.
步骤6：4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 6: Preparation of methyl 4-(4-hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000866
Figure PCTCN2022088560-appb-000866
将6-溴-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-醇(210mg,0.67mmol)用DMF/H 2O混合溶液(11mL，10:1)溶解，加入methyl 4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯(233mg,0.88mmol)，Na 2CO 3(143mg,1.34mmol)和Pd(dppf)Cl 2(25mg,0.03mmol)，在氮气保护下110℃反应过夜，加水(100mL)并搅拌5分钟，用乙酸乙酯(50mLx3)萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 6-Bromo-7-(2-methoxyethoxy)-2-methylquinazolin-4-ol (210 mg, 0.67 mmol) was mixed with DMF/H 2 O (11 mL, 10:1) Dissolve, add methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-ene-1-carboxylate (233mg , 0.88 mmol), Na 2 CO 3 (143 mg, 1.34 mmol) and Pd(dppf)Cl 2 (25 mg, 0.03 mmol), reacted at 110° C. overnight under nitrogen protection, added water (100 mL) and stirred for 5 minutes, then added with ethyl acetate. Ester (50 mL×3) was extracted, the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (MeOH:DCM=1:9) to obtain 4-(4- Hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝373.1. LC-MS: (ESI, m/z): [M+H] + = 373.1.
步骤7：(1R,4R)-4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 7: Methyl (1R,4R)-4-(4-hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate Preparation of esters
Figure PCTCN2022088560-appb-000867
Figure PCTCN2022088560-appb-000867
在高压釜中，加入4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(500mg,1.3mmol)，用MeOH(30mL)溶解后，加入Pd(OH) 2/C(150mg,20％)，在氢气环境中(2MPa)于70℃反应48小时，过滤，减压浓缩，粗品使用反相制备分离得到(1R,4R)-4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 In an autoclave, add methyl 4-(4-hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate Ester (500 mg, 1.3 mmol), dissolved in MeOH (30 mL), added Pd(OH) 2 /C (150 mg, 20%), reacted at 70 °C for 48 hours in a hydrogen atmosphere (2 MPa), filtered and concentrated under reduced pressure , the crude product was isolated by reverse-phase preparation to obtain (1R,4R)-4-(4-hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane- Methyl 1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝375.2. LC-MS: (ESI, m/z): [M+H] + = 375.2.
步骤8：(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 8: (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino Preparation of )-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000868
Figure PCTCN2022088560-appb-000868
将(1R,4R)-4-(4-羟基-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(80mg,0.21mmol)溶于DMF(5mL)，加入BOP(123mg,0.28mmol)和DBU(81mg,0.53mmol)，室温搅拌0.5h后，加入(R)- (3-(1-氨基乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(70mg,0.23mmol)，并移至70℃油浴中反应过夜，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相纯化得到(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。(1R,4R)-4-(4-hydroxy-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester ( 80mg, 0.21mmol) was dissolved in DMF (5mL), BOP (123mg, 0.28mmol) and DBU (81mg, 0.53mmol) were added, and after stirring at room temperature for 0.5h, (R)-(3-(1-aminoethyl) was added -5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (70 mg, 0.23 mmol), and moved to a 70°C oil bath to react overnight, added water (50 mL) and stirred for 5 minutes, then added with ethyl acetate (30 mL×3 ) extraction, the organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by reverse phase to obtain (1R,4R)-4-(4-(((R)-1 -(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-(2-methoxyethoxy)-2-methylquinazole olin-6-yl)cyclohexane-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝661.2. LC-MS: (ESI, m/z): [M+H] + = 661.2.
步骤9：(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 9: (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino Preparation of )-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000869
Figure PCTCN2022088560-appb-000869
将(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(66mg,0.10mmol)溶于THF/H 2O混合溶液(15mL,2:1)中，加入LiOH(48mg,2.0mmol)，50℃搅拌过夜，加水(20mL)，用浓盐酸调节pH至6，用MeOH/DCM(10％,30mLx3)萃取，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相纯化得到(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- Methyl 7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate (66 mg, 0.10 mmol) was dissolved in a mixed solution of THF/H 2 O (15mL, 2:1), add LiOH (48mg, 2.0mmol), stir at 50°C overnight, add water (20mL), adjust pH to 6 with concentrated hydrochloric acid, extract with MeOH/DCM (10%, 30mLx3), It was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by reverse phase to obtain (1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5 -(trifluoromethyl)phenyl)ethyl)amino)-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝647.4. LC-MS: (ESI, m/z): [M+H] + = 647.4.
步骤10：(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 10: (3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-Chloro-3-(2,4-dioxotetrahydro) Pyrimidine-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-(2-methyl) Preparation of tert-butyl oxyethoxy)-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000870
Figure PCTCN2022088560-appb-000870
将(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羧酸(50mg,0.08mmol)溶于DMF(5mL)，加入1-(2-氯-5-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(48mg,0.10mmol)，DIEA(52mg,0.40mmol)和pyBOP(50mg,0.10mmol)，室温反应1h，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)萃取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。(1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- 7-(2-Methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (50 mg, 0.08 mmol) was dissolved in DMF (5 mL), 1-( 2-Chloro-5-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H )-dione (48 mg, 0.10 mmol), DIEA (52 mg, 0.40 mmol) and pyBOP (50 mg, 0.10 mmol), reacted at room temperature for 1 h, added water (50 mL) and stirred for 5 min, extracted with ethyl acetate (30 mL×3), saturated The organic phase was washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by reverse-phase preparation to obtain (3-((R)-1-((6-((1R,4R)- 4-(4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane Alk-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-(2-methoxyethoxy)-2-methylquinazolin-4-yl)amino)ethyl) - tert-butyl 5-(trifluoromethyl)phenyl)carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝1130.4. LC-MS: (ESI, m/z): [M+H] + = 1130.4.
步骤11：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 11: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-(2-methoxyethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl) - Preparation of 3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000871
Figure PCTCN2022088560-appb-000871
将(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸 叔丁酯(80mg,0.07mmol)溶于DCM(5mL)中，加入TFA(1mL)，室温搅拌1小时，减压浓缩后，加入MeOH/DCM(1:9,20mL)溶解，再加入饱和碳酸氢钠水溶液(20mL)调节pH至中性，搅拌10分钟后，用MeOH/DCM(1:9,20mL×3)萃取，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-(2-甲氧基乙氧基)-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((R)-1-((6-((1R,4R)-4-(4-((3-(4-chloro-3-(2,4-dioxotetrahydropyrimidine- 1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-(2-methoxy Ethoxy)-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (80 mg, 0.07 mmol) was dissolved in DCM (5 mL) ), added TFA (1 mL), stirred at room temperature for 1 hour, concentrated under reduced pressure, added MeOH/DCM (1:9, 20 mL) to dissolve, then added saturated aqueous sodium bicarbonate solution (20 mL) to adjust pH to neutral, stirred for 10 After min, it was extracted with MeOH/DCM (1:9, 20 mL×3), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(9-(((4- ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-(2-methoxy Ethoxy)-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3- carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1030.5. LC-MS: (ESI, m/z): [M+H] + = 1030.5.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.12(d,J＝7.7Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.55(d,J＝1.8Hz,1H),7.39(d,J＝8.2Hz,1H),6.98(s,1H),6.87(s,1H),6.85(s,1H),6.70(s,1H),5.61–5.48(m,3H),4.22-4.17(m,2H),3.75(d,J＝4.6Hz,3H),3.65–3.52(m,3H),3.51-3.41(m,4H),3.36(s,3H),3.02-2.88(m,1H),2.79-2.71(m,2H),2.68-2.60(m,1H),2.29-2.38(m,5H),2.28-2.21(m,2H),2.16-2.06(m,2H),1.95-1.85(m,2H),1.84-1.80(m,2H),1.76-1.19(m,18H),1.17-0.95(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.12(d, J=7.7Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.55(d,J＝1.8Hz,1H),7.39(d,J＝8.2Hz,1H),6.98(s,1H),6.87(s,1H),6.85(s,1H),6.70(s, 1H), 5.61-5.48(m, 3H), 4.22-4.17(m, 2H), 3.75(d, J=4.6Hz, 3H), 3.65-3.52(m, 3H), 3.51-3.41(m, 4H) ,3.36(s,3H),3.02-2.88(m,1H),2.79-2.71(m,2H),2.68-2.60(m,1H),2.29-2.38(m,5H),2.28-2.21(m, 2H), 2.16-2.06(m, 2H), 1.95-1.85(m, 2H), 1.84-1.80(m, 2H), 1.76-1.19(m, 18H), 1.17-0.95(m, 4H).
实施例44：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 44: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) (yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl )piperidine-1-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯的制备Step 1: 4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoro Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl Preparation of benzyl) piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000872
Figure PCTCN2022088560-appb-000872
(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(100mg,0.17mmol)溶解于DMF(8mL)中，4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯(72mg,0.2mmol)，HATU(90mg,0.23mmol)与DIEA(64mg,0.5mmol)分别加入。反应液室温搅拌5小时后，向反应液中加入水(50mL)，用乙酸乙酯(30mLx3)萃取，有机相用饱和食盐水(50mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯。(1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (100 mg, 0.17 mmol) was dissolved in DMF (8 mL), 4-((2-(piperidine-4 -yl)ethoxy)methyl)piperidine-1-carboxylate benzyl ester (72 mg, 0.2 mmol), HATU (90 mg, 0.23 mmol) and DIEA (64 mg, 0.5 mmol) were added separately. After the reaction solution was stirred at room temperature for 5 hours, water (50 mL) was added to the reaction solution, extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure . The crude product was purified by column chromatography (methanol:dichloromethane=1:9) to obtain 4-((2-(1-((1R,4R)-4-(4-((((R)-1-(3- ((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝945.5. LC-MS: (ESI, m/z): [M+H] + = 945.5.
步骤2：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹啉唑-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 2: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidin-4-yl Preparation of methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)quinolinazol-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000873
Figure PCTCN2022088560-appb-000873
4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸苄酯(100mg,0.11mmol)用乙酸乙酯(8mL)溶解，加入Pd(OH) 2/C(50mg,0.14mmol)，在氢气氛围下升温至70℃搅拌过夜。反应液冷却至室温，过滤，滤液减压浓缩得到(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹啉唑-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。 4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine Benzyl pyridine-1-carboxylate (100 mg, 0.11 mmol) was dissolved in ethyl acetate (8 mL), Pd(OH) 2 /C (50 mg, 0.14 mmol) was added, and the temperature was raised to 70° C. and stirred overnight under a hydrogen atmosphere. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4- (2-(Piperidin-4-ylmethoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)quinolinazol-4-yl)amino)ethyl)-5-(trifluoromethyl)benzene base) tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝811.5. LC-MS: (ESI, m/z): [M+H] + = 811.5.
步骤3：(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 3: (3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)-4-fluorobenzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Preparation of tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000874
Figure PCTCN2022088560-appb-000874
(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羰基)环己基)喹啉唑-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(80mg,0.098mmol)用DMSO(8mL)溶解，加入1-(2-氟-5-(五氟苯甲酰)苯基)二氢嘧啶-2,4(1H,3H)-二酮(40mg,0.098mmol)和DIEA(40mg,0.28mmol)，室温下搅拌2小时。反应液加入水(100mL)，用乙酸乙酯(30mLx3)萃取，有机相用饱和食盐水(50mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。(3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(2-(piperidin-4-ylmethoxy )ethyl)piperidine-1-carbonyl)cyclohexyl)quinolinazol-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (80 mg, 0.098 mmol) Dissolve with DMSO (8 mL), add 1-(2-fluoro-5-(pentafluorobenzoyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (40 mg, 0.098 mmol) and DIEA (40 mg, 0.28 mmol) and stirred at room temperature for 2 hours. The reaction solution was added with water (100 mL), extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (methanol: two Chloromethane=1:9) to obtain (3-((R)-1-(((6-((1R,4R)-4-(4-(2-((1-(3-(2,4- Dioxotetrahydropyrimidine-1(2H)-yl)-4-fluorobenzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methyl Oxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1045.3. LC-MS: (ESI, m/z): [M+H] + = 1045.3.
步骤4：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl) Preparation of piperidine-1-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000875
Figure PCTCN2022088560-appb-000875
(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(50mg,0.047mmol)用二氯甲烷(5mL)溶解，加入三氟乙酸(2mL)，室温下搅拌2小时。反应液直接减压浓缩，粗品经Prep-HPLC纯化得到1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((R)-1-((6-((1R,4R)-4-(4-(2-((1-(3-(2,4-dioxotetrahydropyrimidine-1( 2H)-yl)-4-fluorobenzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazole Lin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (50 mg, 0.047 mmol) was dissolved in dichloromethane (5 mL) and trifluoroacetic acid (2 mL) was added , and stirred at room temperature for 2 hours. The reaction solution was directly concentrated under reduced pressure, and the crude product was purified by Prep-HPLC to obtain 1-(5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-() 3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine- 4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝945.4. LC-MS: (ESI, m/z): [M+H] + = 945.4.
1H NMR(400MHz,MeOD)δ10.52(s,1H),8.19–7.99(m,2H),7.49(d,J＝7.9Hz,1H),7.37(d,J＝8.3Hz,2H),6.99(s,1H),6.87(s,1H),6.85(s,1H),6.70(s,1H),5.65–5.47(m,3H),4.50-4.33(m,2H),3.96-3.85(m,4H),3.74(t,J＝6.7Hz,2H),3.41(t,J＝6.4Hz,2H),3.23(d,J＝6.2Hz,2H),3.08–2.89(m,3H),2.72(t,J＝6.7Hz,2H),2.69-2.60(m,1H),2.40-2.30(m,4H),1.99-1.37(m,22H),1.16-0.94(m,4H). 1 H NMR(400MHz,MeOD)δ10.52(s,1H),8.19-7.99(m,2H),7.49(d,J=7.9Hz,1H),7.37(d,J=8.3Hz,2H), 6.99(s, 1H), 6.87(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.65-5.47(m, 3H), 4.50-4.33(m, 2H), 3.96-3.85( m, 4H), 3.74 (t, J=6.7Hz, 2H), 3.41 (t, J=6.4Hz, 2H), 3.23 (d, J=6.2Hz, 2H), 3.08–2.89 (m, 3H), 2.72(t, J＝6.7Hz, 2H), 2.69-2.60(m, 1H), 2.40-2.30(m, 4H), 1.99-1.37(m, 22H), 1.16-0.94(m, 4H).
实施例45：1-(5-(4-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮 Example 45: 1-(5-(4-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)piperidine-1- Carbonyl-2,2,6,6-d 4 )-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羧酸叔丁酯-2,2,6,6-d 4的制备 Step 1: 4-((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)piperidine-1 - Preparation of tert-butyl carboxylate-2,2,6,6-d 4
Figure PCTCN2022088560-appb-000876
Figure PCTCN2022088560-appb-000876
将4-(哌啶-4-基甲氧基)哌啶-1-羧酸叔丁酯-2,2,6,6-d 4(150mg,0.50mmol)用DMF(5mL)溶解，加入(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己 烷-1-羧酸(150mg,0.25mmol)，HATU(123mg,0.32mmol)和DIEA(161mg,1.25mmol)，室温搅拌2小时，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羧酸叔丁酯-2,2,6,6-d 4。 4-(Piperidin-4-ylmethoxy)piperidine-1-carboxylate tert-butyl ester-2,2,6,6- d4 (150 mg, 0.50 mmol) was dissolved in DMF (5 mL), ( 1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7- Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.25 mmol), HATU (123 mg, 0.32 mmol) and DIEA (161 mg, 1.25 mmol), stirred at room temperature for 2 hour, added water (50 mL) and stirred for 5 minutes, extracted with ethyl acetate (30 mL×3), washed the organic phase with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (MeOH). : DCM=1:9) purification to give 4-((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5- (Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy yl)piperidine-1-carboxylate tert-butyl ester-2,2,6,6-d 4 .
LC-MS:(ESI,m/z):[M+H] +＝887.4. LC-MS: (ESI, m/z): [M+H] + = 887.4.
步骤2：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-基)甲酮的制备 Step 2: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)cyclohexyl)(4-(((piperidin-4-yl-2,2,6,6-d 4 )oxy)methyl)piperidine-1- The preparation of ketone
Figure PCTCN2022088560-appb-000877
Figure PCTCN2022088560-appb-000877
将4-((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羧酸叔丁酯-2,2,6,6-d 4(200mg,0.23mmol)溶于DCM(5mL)中，加入TFA(1mL)，室温搅拌2小时，减压浓缩得到((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-基)甲酮，直接用于下一步。 4-((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)piperidine-1-carboxy tert-Butyl acid-2,2,6,6-d 4 (200 mg, 0.23 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, stirred at room temperature for 2 hours, and concentrated under reduced pressure to give ((1R,4R) -4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexyl)(4-(((piperidin-4-yl-2,2,6,6-d 4 )oxy)methyl)piperidin-1-yl)methanone, used directly under step.
LC-MS:(ESI,m/z):[M+H] +＝687.4. LC-MS: (ESI, m/z): [M+H] + = 687.4.
步骤3：1-(5-(4-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 3: 1-(5-(4-((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)piperidine-1-carbonyl Preparation of -2,2,6,6-d 4 )-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000878
Figure PCTCN2022088560-appb-000878
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(((哌啶-4-基-2,2,6,6-d 4)氧)甲基)哌啶-1-基)甲酮(200mg,0.29mmol)溶于DMSO(5mL)，加入DIEA(149mg,1.15mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(100mg,0.23mmol)，室温搅拌2h，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(4-((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)哌啶-1-羰基-2,2,6,6-d 4)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-(((piperidin-4-yl-2,2,6,6- d4 )oxy)methyl)piperidin-1-yl) Methanone (200 mg, 0.29 mmol) was dissolved in DMSO (5 mL), DIEA (149 mg, 1.15 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzene were added Pentafluorophenyl formate (100 mg, 0.23 mmol), stirred at room temperature for 2 h, added water (50 mL) and stirred for 5 min, extracted with ethyl acetate (30 mL×3), washed the organic phase with saturated brine (50 mL), and dried over anhydrous sodium sulfate , filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(4-((1-((1R,4R)-4-(4-((((R)-1-(3-amino) -5-(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl )Methoxy)piperidine-1-carbonyl-2,2,6,6- d4 )-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):(ESI,m/z):[M+H] +＝937.5. LC-MS: (ESI, m/z): (ESI, m/z): [M+H] + = 937.5.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.13(s,1H),8.09(s,1H),7.63(d,J＝8.2Hz,1H),7.57(d,J＝1.9Hz,1H),7.40(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.70(s,1H),5.62–5.50(m,3H),4.42(d,J＝11.5Hz,1H),4.0–3.92(m,4H),3.74(s,1H),3.67–3.47(m,2H),3.29(d,J＝4.5Hz,2H),3.09–2.87(m,2H),2.76-2.73(m,2H),2.67-2.63(m,1H),2.36(s,3H),1.94–1.50(m,17H),1.50–1.38(m,2H),1.16–0.91(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.13(s, 1H), 8.09(s, 1H), 7.63(d, J=8.2Hz, 1H), 7.57(d, J=1.9Hz, 1H), 7.40(dd, J=8.2, 2.0Hz, 1H), 6.99(s, 1H), 6.88(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.62–5.50 (m, 3H), 4.42 (d, J=11.5Hz, 1H), 4.0–3.92 (m, 4H), 3.74 (s, 1H), 3.67–3.47 (m, 2H), 3.29 (d, J=4.5Hz, 2H), 3.09–2.87 (m, 2H), 2.76–2.73 (m, 2H), 2.67–2.63 (m, 1H), 2.36 (s, 3H), 1.94–1.50 (m, 17H) ,1.50–1.38(m,2H),1.16–0.91(m,2H).
实施例46：3-(2-氯-5-(4-((2-(1-(4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)哌啶-2,6-二酮Example 46: 3-(2-Chloro-5-(4-((2-(1-(4-(4-((((R)-1-(4-(2-Chloro-6-((Di Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl )piperidine-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)piperidine-2,6-dione
步骤1：4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-yl)环己-3-烯-1-羧酸甲酯的制备Step 1: 4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6-yl) Preparation of methyl cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000879
Figure PCTCN2022088560-appb-000879
将(R)-1-(4-溴-2-基)乙烷-1-胺(607mg,3mmol)溶于DMF(5mL)，加入BOP(574.6mg,1.3mmol)和DBU(456.0mg,3.0mmol)，反应液在室温下搅拌0.5小时，接着向反应液中加入4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(328mg,1mmol)并升温至70℃反应16小时。反应液用水(50mL)稀释，乙酸乙酯萃取(30mL×3)，合并上层有机相并用饱和食盐水洗，无水Na 2SO 4干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-yl)环己-3-烯-1-羧酸甲酯。 (R)-1-(4-Bromo-2-yl)ethane-1-amine (607 mg, 3 mmol) was dissolved in DMF (5 mL), BOP (574.6 mg, 1.3 mmol) and DBU (456.0 mg, 3.0 mmol) were added mmol), the reaction solution was stirred at room temperature for 0.5 hours, and then 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene- 1-Carboxylic acid methyl ester (328 mg, 1 mmol) was heated to 70 °C and reacted for 16 hours. The reaction solution was diluted with water (50 mL), extracted with ethyl acetate (30 mL×3), the upper organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The crude product was subjected to column chromatography (MeOH:DCM). =1:9) purification to give 4-(4-(((R)-1-(4-bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl) cyclohex-3-ene-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝516.1. LC-MS: (ESI, m/z): [M+H] + = 516.1.
步骤2：4-(4-(((R)-1-(4-(2-氯-6-苯甲醛)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 2: 4-(4-(((R)-1-(4-(2-chloro-6-benzaldehyde)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methyl Preparation of methyl quinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000880
Figure PCTCN2022088560-appb-000880
将3-氯-2-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)苯甲醛(206mg,0.77mmol)和4-(4-(((R)-1-(4-溴噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-yl)环己-3-烯-1-羧酸甲酯(400mg,0.77mmol)溶于DMF/H 2O(3mL/0.3mL)，加入Pd(dppf)Cl 2(100mg)和K 2CO 3(214mg,1.55mmol)，置换氮气，在氮气保护下100℃搅拌2小时。反应结束后反应液用水(50mL)稀释，乙酸乙酯萃取(30mL×3)，合并有机相并用饱和食盐水洗，无水Na 2SO 4干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-(4-(((R)-1-(4-(2-氯-6-苯甲醛)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 3-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)benzaldehyde (206 mg, 0.77 mmol) and 4-(4- (((R)-1-(4-Bromothiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6-yl)cyclohex-3-ene-1 - Methyl carboxylate (400 mg, 0.77 mmol) was dissolved in DMF/H 2 O (3 mL/0.3 mL), Pd(dppf)Cl 2 (100 mg) and K 2 CO 3 (214 mg, 1.55 mmol) were added, nitrogen was replaced, Stir at 100°C for 2 hours under nitrogen protection. After the reaction, the reaction solution was diluted with water (50 mL), extracted with ethyl acetate (30 mL×3), the organic phases were combined and washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (MeOH). : DCM=1:9) to obtain 4-(4-(((R)-1-(4-(2-chloro-6-benzaldehyde)thiophen-2-yl)ethyl)amino)-7-methyl Methyl oxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝576.3. LC-MS: (ESI, m/z): [M+H] + = 576.3.
步骤3：4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 3: 4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino) Preparation of -7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester
Figure PCTCN2022088560-appb-000881
Figure PCTCN2022088560-appb-000881
将4-(4-(((R)-1-(4-(2-氯-6-苯甲醛)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(130mg,0.22mmol)溶于1,2-二氯乙烷(5mL)，加入三乙酰氧基硼氢化钠(143mg,0.68mmol)，反应液80℃搅拌1小时。反应液用水(50ml)稀释，二氯甲烷萃取(30mL×3)，合并有机相，无水Na 2SO 4干燥，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:19)纯化得到4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 4-(4-(((R)-1-(4-(2-chloro-6-benzaldehyde)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinoline Methyl oxazolin-6-yl)cyclohex-3-ene-1-carboxylate (130mg, 0.22mmol) was dissolved in 1,2-dichloroethane (5mL), sodium triacetoxyborohydride (143mg) was added , 0.68 mmol), the reaction solution was stirred at 80 °C for 1 hour. The reaction solution was diluted with water (50 ml), extracted with dichloromethane (30 mL×3), the organic phases were combined, dried over anhydrous Na 2 SO 4 , concentrated under reduced pressure, and the crude product was purified by column chromatography (MeOH:DCM=1:19) to obtain 4-(4-(((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7- Methyl methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝605.3. LC-MS: (ESI, m/z): [M+H] + = 605.3.
步骤4：4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸的制备Step 4: 4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino) Preparation of -7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid
Figure PCTCN2022088560-appb-000882
Figure PCTCN2022088560-appb-000882
将4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(170mg,0.28mmol)用MeOH/H 2O(2mL/0.2mL)溶解，加入LiOH(52mg,1.3mmol)，反应液加热至60℃搅拌1小时。冷却，用稀盐酸(1.0mol/L)调节pH至3-4，再加入NaHCO 3饱和溶液调节pH至7-8，乙酸乙酯萃取(30mL×3)，合并有机相，用无水Na 2SO 4干燥，过滤，减压浓缩得到(R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸。 4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester (170 mg, 0.28 mmol) was dissolved in MeOH/H 2 O (2 mL/0.2 mL), LiOH (52 mg, 1.3 mmol) was added, and the reaction solution was heated to 60°C and stirred for 1 hour. Cool, adjust the pH to 3-4 with dilute hydrochloric acid (1.0 mol/L), then add NaHCO 3 saturated solution to adjust the pH to 7-8, extract with ethyl acetate (30 mL×3), combine the organic phases, use anhydrous Na 2 Dry over SO4 , filter, and concentrate under reduced pressure to give (R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl) Thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝591.3. LC-MS: (ESI, m/z): [M+H] + = 591.3.
步骤5：3-(2-氯-5-(4-((2-(1-(4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)哌啶-2,6-二酮的制备Step 5: 3-(2-Chloro-5-(4-((2-(1-(4-(4-((((R)-1-(4-(2-Chloro-6-((dimethyl) (ylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl) Preparation of piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)piperidine-2,6-dione
Figure PCTCN2022088560-appb-000883
Figure PCTCN2022088560-appb-000883
将4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸(125mg,0.22mmol)和3-(2-氯-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)哌啶-2,6-二酮(108mg,0.22mmol)用DMF(3mL)溶解，加入HATU(96mg,0.25mmol)和DIEA(82mg,0.64mmol)，室温下搅拌1小时。反应液用水(50mL)稀释，乙酸乙酯萃取(30mL×3)，有机相用饱和食盐水洗，无水Na 2SO 4干燥，过滤，减压浓缩，粗品使用Prep-HPLC纯化得到产品3-(2-氯-5-(4-((2-(1-(4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)哌啶-2,6-二酮。 4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid (125 mg, 0.22 mmol) and 3-(2-chloro-5-(4-((2 -(Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)piperidine-2,6-dione (108 mg, 0.22 mmol) was dissolved in DMF (3 mL) and HATU was added (96 mg, 0.25 mmol) and DIEA (82 mg, 0.64 mmol) and stirred at room temperature for 1 hour. The reaction solution was diluted with water (50 mL), extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine, dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure. The crude product was purified by Prep-HPLC to obtain the product 3-( 2-Chloro-5-(4-((2-(1-(4-(4-(((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)) Phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl )ethoxy)methyl)piperidine-1-carbonyl)phenyl)piperidine-2,6-dione.
LC-MS:(ESI,m/z):[M+H] +＝1049.3. LC-MS: (ESI, m/z): [M+H] + = 1049.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.41(s,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.48–7.30(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.01–5.89(m,1H),5.83(s,1H),4.47-4.37(m,1H),3.99-3.91(m,1H),3.86(s,3H),3.74(s,1H),3.68-3.52(m,2H),3.44-3.37(m,2H),3.26-3.18(m,3H),3.18-2.96(m,3H),2.90-2.82(m,1H),2.81-2.70(m,2H),2.43(s,3H),2.39-2.29(m,2H),2.25-2.16(m,1H),2.03(s,6H),1.89-1.55(m,10H),1.49-1.40(m,2H),1.30-1.20(m,2H),1.20–0.95(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.41(s, 1H), 8.05(s, 1H), 7.63(d, J=8.2Hz, 1H), 7.54(s, 1H), 7.48–7.30(m, 4H), 7.24(s, 1H), 7.02(s, 1H), 6.96(s, 1H), 6.01–5.89(m, 1H), 5.83(s, 1H), 4.47 -4.37(m, 1H), 3.99-3.91(m, 1H), 3.86(s, 3H), 3.74(s, 1H), 3.68-3.52(m, 2H), 3.44-3.37(m, 2H), 3.26 -3.18(m,3H),3.18-2.96(m,3H),2.90-2.82(m,1H),2.81-2.70(m,2H),2.43(s,3H),2.39-2.29(m,2H) ,2.25-2.16(m,1H),2.03(s,6H),1.89-1.55(m,10H),1.49-1.40(m,2H),1.30-1.20(m,2H),1.20–0.95(m, 4H).
实施例47：(1R,4R)-N-(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺Example 47: (1R,4R)-N-(3-(1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidine -4-yl)propyl)-4-(7-methoxy-2-methyl-4-(((R)-1-(4-(2-((methylamino)methyl)phenyl) )thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-carboxamide
步骤1：4-(3-羟基丙基)哌啶-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(3-hydroxypropyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000884
Figure PCTCN2022088560-appb-000884
于0℃下向3-(哌啶-4-基)丙-1-醇(5.00g,34.91mmol)的THF(20mL)溶液中加入CbzCl(5.40ml,38.40mmol)，反应1小时反应完成后，反应液用饱和NaHCO 3水溶液(50mL)淬灭，并用乙酸乙酯(100mLx3) 萃取。合并有机相并用盐水(100mL)洗涤，经硫酸钠干燥，过滤，滤液浓缩。粗品通过硅胶柱层析纯化(MeOH:DCM＝1:100～1:10)，得浅黄色油状的4-(3-羟丙基)哌啶-1-羧酸苄酯。 To a solution of 3-(piperidin-4-yl)propan-1-ol (5.00 g, 34.91 mmol) in THF (20 mL) was added CbzCl (5.40 ml, 38.40 mmol) at 0°C, and the reaction was completed for 1 hour. , the reaction solution was quenched with saturated aqueous NaHCO 3 (50 mL), and extracted with ethyl acetate (100 mL×3). The organic phases were combined and washed with brine (100 mL), dried over sodium sulfate, filtered and the filtrate concentrated. The crude product was purified by silica gel column chromatography (MeOH:DCM=1:100～1:10) to obtain benzyl 4-(3-hydroxypropyl)piperidine-1-carboxylate as pale yellow oil.
LC-MS:(ESI,m/z):[M+H] +＝278.2. LC-MS: (ESI, m/z): [M+H] + = 278.2.
步骤2：4-(3-氧代丙基)哌啶-1-羧酸苄酯的制备Step 2: Preparation of benzyl 4-(3-oxopropyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000885
Figure PCTCN2022088560-appb-000885
于0℃下向4-(3-羟丙基)哌啶-1-甲酸苄酯(3.00g,10.8mmol)的DCM(60mL)溶液中加入Dess-Martin(5.50g,13.0mmol)，反应1小时。反应完成后，反应液用饱和Na 2S 2O 3(50mL)和饱和NaHCO 3(50mL)淬灭，并用DCM(80mLx3)萃取。合并有机相并用盐水(100mL)洗涤，经硫酸钠干燥，过滤并旋干。粗品通过硅胶色谱法纯化(EA:PE＝3:17～3:7)得到4-(3-氧代丙基)哌啶-1-羧酸苄酯。 To a solution of benzyl 4-(3-hydroxypropyl)piperidine-1-carboxylate (3.00 g, 10.8 mmol) in DCM (60 mL) was added Dess-Martin (5.50 g, 13.0 mmol) at 0°C, reaction 1 Hour. After completion of the reaction, the reaction was quenched with saturated Na 2 S 2 O 3 (50 mL) and saturated NaHCO 3 (50 mL), and extracted with DCM (80 mL×3). The organic phases were combined and washed with brine (100 mL), dried over sodium sulfate, filtered and spin-dried. The crude product was purified by silica gel chromatography (EA:PE=3:17-3:7) to give benzyl 4-(3-oxopropyl)piperidine-1-carboxylate.
1H NMR(400MHz,CDCl 3)δ9.78(s,1H),7.38-7.28(m,5H),5.12(s,2H),4.28-4.02(m,2H),2.90-2.65(m,2H),2.51-2.42(m,2H),1.74-1.54(m,4H),1.51-1.37(m,1H),1.21-1.03(m,2H). 1 H NMR (400MHz, CDCl 3 ) δ 9.78(s, 1H), 7.38-7.28(m, 5H), 5.12(s, 2H), 4.28-4.02(m, 2H), 2.90-2.65(m, 2H) ), 2.51-2.42(m, 2H), 1.74-1.54(m, 4H), 1.51-1.37(m, 1H), 1.21-1.03(m, 2H).
步骤3：4-(3-(甲基氨基)丙基)哌啶-1-羧酸苄酯的制备Step 3: Preparation of benzyl 4-(3-(methylamino)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000886
Figure PCTCN2022088560-appb-000886
向4-(3-氧代丙基)哌啶-1-羧酸苄酯(1.50g,5.45mmol)的THF(10mL)溶液中加入甲胺(846mg,27.24mmol)和AcOH(0.1mL)，并在30℃下反应4小时，然后加入NaBH 3CN(684mg,10.90mmol)继续反应16小时。反应完成后，反应液用饱和NaHCO 3(50mL)淬灭并用乙酸乙酯(100mLx3)萃取。合并有机相并用盐水(100mL)洗涤，经硫酸钠干燥，过滤并旋干。粗品通过硅胶色谱法纯化(用NH 3/MeOH:DCM＝1:9～2:8)得到4-(3-(甲基氨基)丙基)哌啶-1-羧酸苄酯。 To a solution of benzyl 4-(3-oxopropyl)piperidine-1-carboxylate (1.50 g, 5.45 mmol) in THF (10 mL) was added methylamine (846 mg, 27.24 mmol) and AcOH (0.1 mL), The reaction was carried out at 30°C for 4 hours, and then NaBH 3 CN (684 mg, 10.90 mmol) was added to continue the reaction for 16 hours. After completion of the reaction, the reaction was quenched with saturated NaHCO 3 (50 mL) and extracted with ethyl acetate (100 mL×3). The organic phases were combined and washed with brine (100 mL), dried over sodium sulfate, filtered and spin-dried. The crude product was purified by silica gel chromatography (with NH3 /MeOH:DCM=1:9-2:8) to give benzyl 4-(3-(methylamino)propyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝291.7. LC-MS: (ESI, m/z): [M+H] + = 291.7.
步骤4：4-(3-((叔丁氧羰基)(甲基)氨基)丙基)哌啶-1-甲酸苄酯的制备Step 4: Preparation of benzyl 4-(3-((tert-butoxycarbonyl)(methyl)amino)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000887
Figure PCTCN2022088560-appb-000887
向4-(3-(甲基氨基)丙基)哌啶-1-羧酸苄酯(295mg,1.02mol)的DCM(3mL)溶液中加入(Boc) 2O(1.2mL,5.10mmol)并于室温反应16小时。反应完成后，反应液用水(50mL)淬灭并用乙酸乙酯(50mLx3)萃取。合并有机相并用盐水(100mL)洗涤，经硫酸钠干燥，过滤并旋干。粗品通过硅胶色谱法纯化(NH 3/MeOH:DCM＝1:19～1:9)得到4-(3-((叔丁氧羰基)(甲基)氨基)丙基)哌啶-1-甲酸苄酯。 To a solution of benzyl 4-(3-(methylamino)propyl)piperidine-1-carboxylate (295 mg, 1.02 mol) in DCM (3 mL) was added (Boc)2O ( 1.2 mL, 5.10 mmol) and The reaction was carried out at room temperature for 16 hours. After completion of the reaction, the reaction solution was quenched with water (50 mL) and extracted with ethyl acetate (50 mL×3). The organic phases were combined and washed with brine (100 mL), dried over sodium sulfate, filtered and spin-dried. The crude product was purified by silica gel chromatography ( NH3 /MeOH:DCM=1:19～1:9) to give 4-(3-((tert-butoxycarbonyl)(methyl)amino)propyl)piperidine-1-carboxylic acid benzyl ester.
LC-MS:(ESI,m/z):[M-100+H] +＝291.2. LC-MS: (ESI, m/z): [M-100+H] + = 291.2.
步骤5：甲基(3-哌啶-4-基)丙基)羧酸叔丁酯的制备Step 5: Preparation of tert-butyl methyl(3-piperidin-4-yl)propyl)carboxylate
Figure PCTCN2022088560-appb-000888
Figure PCTCN2022088560-appb-000888
向4-(3-((叔丁氧基羰基)(甲基)氨基)丙基)哌啶-1-甲酸苄酯(291mg,0.75mmol)的MeOH(5mL)溶液中加入Pd/C(80mg)并用氢气置换三次，室温反应16小时。将反应液旋干，得到粗品甲基(3-哌啶-4-基)丙基)羧酸叔丁酯，无需进一步纯化即可用于下一步反应。To a solution of benzyl 4-(3-((tert-butoxycarbonyl)(methyl)amino)propyl)piperidine-1-carboxylate (291 mg, 0.75 mmol) in MeOH (5 mL) was added Pd/C (80 mg) ) and replaced with hydrogen three times, and reacted at room temperature for 16 hours. The reaction solution was spun dry to obtain crude tert-butyl methyl(3-piperidin-4-yl)propyl)carboxylate, which was used in the next reaction without further purification.
LC-MS:(ESI,m/z):[M+H] +＝257.2. LC-MS: (ESI, m/z): [M+H] + = 257.2.
步骤6：(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羧酸叔丁酯的制备Step 6: (3-(1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)propyl)( Preparation of tert-butyl methyl)carboxylate
Figure PCTCN2022088560-appb-000889
Figure PCTCN2022088560-appb-000889
向甲基(3-(哌啶-4-基)丙基)氨基甲酸叔丁酯(150mg,0.59mmol)的DMSO(2mL)溶液中加入DIEA(232mg,1.8mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(381mg,0.88mmol)，并于室温下反应16小时。反应完成后，反应液用水(50mL)淬灭并用乙酸乙酯(50mLx3)萃取。合并有机相并用盐水(100mL)洗涤，经硫酸钠干燥，过滤并旋干。粗品通过硅胶色谱法纯化(用NH 3/MeOH:DCM＝1:19～1:9)得到目标化合物(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羧酸叔丁酯。 To a solution of tert-butyl methyl(3-(piperidin-4-yl)propyl)carbamate (150 mg, 0.59 mmol) in DMSO (2 mL) was added DIEA (232 mg, 1.8 mmol) and 4-chloro-3- (2,4-Dioxotetrahydropyrimidin-1(2H)-yl)pentafluorophenyl benzoate (381 mg, 0.88 mmol) and reacted at room temperature for 16 hours. After completion of the reaction, the reaction solution was quenched with water (50 mL) and extracted with ethyl acetate (50 mL×3). The organic phases were combined and washed with brine (100 mL), dried over sodium sulfate, filtered and spin-dried. The crude product was purified by silica gel chromatography (with NH3 /MeOH:DCM=1:19～1:9) to give the title compound (3-(1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine)) -1(2H)-yl)benzoyl)piperidin-4-yl)propyl)(methyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+Na] +＝529.1. LC-MS: (ESI, m/z): [M+Na] + = 529.1.
步骤7：1-(2-氯-5-(4-(3-(甲基氨基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(2-Chloro-5-(4-(3-(methylamino)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dihydropyrimidine Preparation of ketones
Figure PCTCN2022088560-appb-000890
Figure PCTCN2022088560-appb-000890
将化合物(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羧酸叔丁酯(256mg,0.50mmol)溶于DCM(2mL)中，室温下加入TFA(1mL)，反应0.5小时。将反应液液浓缩，得到粗品1-(2-氯-5-(4-(3-(甲基氨基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，无需进一步纯化用于下一步反应。The compound (3-(1-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)propyl)(methyl (256 mg, 0.50 mmol) was dissolved in DCM (2 mL), TFA (1 mL) was added at room temperature, and the reaction was carried out for 0.5 h. The reaction liquid was concentrated to obtain crude 1-(2-chloro-5-(4-(3-(methylamino)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H ,3H)-dione and was used in the next reaction without further purification.
LC-MS:(ESI,m/z):[M+H] +＝407.0. LC-MS: (ESI, m/z): [M+H] + = 407.0.
步骤8：(2-(5-((R)-1-((6-((1R,4R)-4-((3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苯基)(甲基)羧酸叔丁酯的制备Step 8: (2-(5-((R)-1-((6-((1R,4R)-4-((3-(1-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)propyl)(methyl)carbonyl)cyclohexyl)-7-methoxy-2-methylquinazoline- Preparation of 4-yl)amino)ethyl)thiophen-3-yl)phenyl)(methyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000891
Figure PCTCN2022088560-appb-000891
向化合物(1R,4R)-4-(4-(((R)-1-(4-(2-(((叔丁氧羰基)(甲基)氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(229mg,0.36mmol)的DMF(3mL)溶液中加入1-(2-氯-5-(4-(3-(甲基氨基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(216mg,0.53mmol)，TCFH(249mg,0.89mmol)和NMI(146mg,1.78mmol)，并于室温下反应16小时。反应完成后，反应液用水(20mL)淬灭并用乙酸乙酯(20mLx3)萃取。合并有机相并用盐水(50mL)洗涤，经硫酸钠干燥，过滤并真空浓缩。粗品通过硅胶色谱法纯化(NH 3/MeOH:DCM＝1:19～1:9)得到目标化合物(2-(5-((R)-1-((6-((1R,4R)-4-((3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苯基)(甲基)羧酸叔丁酯。 To compound (1R,4R)-4-(4-(((R)-1-(4-(2-(((tert-butoxycarbonyl)(methyl)amino)methyl)phenyl)thiophene-2 -yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (229 mg, 0.36 mmol) in DMF (3 mL) was added 1 -(2-Chloro-5-(4-(3-(methylamino)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (216 mg, 0.53 mmol), TCFH (249 mg, 0.89 mmol) and NMI (146 mg, 1.78 mmol), and reacted at room temperature for 16 hours. After completion of the reaction, the reaction solution was quenched with water (20 mL) and extracted with ethyl acetate (20 mL×3). The organic phases were combined and washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography (NH 3 /MeOH:DCM=1:19～1:9) to obtain the target compound (2-(5-((R)-1-((6-((1R,4R)-4 -((3-(1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)propyl)(methyl (methyl)carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)phenyl)(methyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1033.2. LC-MS: (ESI, m/z): [M+H] + = 1033.2.
步骤9：(1R,4R)-N-(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺的制备Step 9: (1R,4R)-N-(3-(1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidine- 4-yl)propyl)-4-(7-methoxy-2-methyl-4-(((R)-1-(4-(2-((methylamino)methyl)phenyl) Preparation of thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-carboxamide
Figure PCTCN2022088560-appb-000892
Figure PCTCN2022088560-appb-000892
在室温下向化合物(2-(5-((R)-1-((6-((1R,4R)-4-((3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)(甲基)羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苯基)(甲基)羧酸叔丁酯(107mg,0.10mmol)的DCM(2mL)溶液中加入TFA(1mL)，并反应0.5小时。将反应液液浓缩得粗品，通过高效液相制备色谱纯化得到目标化合物(1R,4R)-N-(3-(1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺。Compound (2-(5-((R)-1-((6-((1R,4R)-4-(((3-(1-(4-chloro-3-(2,4- Dioxotetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)propyl)(methyl)carbonyl)cyclohexyl)-7-methoxy-2-methylquinazole Lin-4-yl)amino)ethyl)thiophen-3-yl)phenyl)(methyl)carboxylate tert-butyl ester (107 mg, 0.10 mmol) in DCM (2 mL) was added TFA (1 mL) and reacted 0.5 hours. The reaction liquid was concentrated to obtain the crude product, which was purified by high performance liquid preparative chromatography to obtain the target compound (1R,4R)-N-(3-(1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)benzoyl)piperidin-4-yl)propyl)-4-(7-methoxy-2-methyl-4-(((R)-1-(4- (2-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-carboxamide.
LC-MS:(ESI,m/z):[M+H] +＝933.4. LC-MS: (ESI, m/z): [M+H] + = 933.4.
1H NMR(400MHz,CD 3OD)δ7.99(s,1H),7.66-7.58(m,1H),7.54-7.48(m,1H),7.43-7.36(m,2H),7.33-7.26(m,3H),7.18(d,J＝1.2Hz,1H),7.15-7.11(m,1H),7.01(m,1H),6.08-6.01(m,1H),4.65-4.53(m,1H),3.95(s,3H),3.81-3.69(m,5H),3.48-3.34(m,2H),3.16-3.04(m,4H),2.95-2.68(m,5H),2.52(s,3H),2.22(s,3H),2.00-1.57(m,16H),1.35-1.11(m,4H). 1 H NMR (400MHz, CD 3 OD) δ 7.99(s, 1H), 7.66-7.58(m, 1H), 7.54-7.48(m, 1H), 7.43-7.36(m, 2H), 7.33-7.26( m,3H),7.18(d,J＝1.2Hz,1H),7.15-7.11(m,1H),7.01(m,1H),6.08-6.01(m,1H),4.65-4.53(m,1H) ,3.95(s,3H),3.81-3.69(m,5H),3.48-3.34(m,2H),3.16-3.04(m,4H),2.95-2.68(m,5H),2.52(s,3H) ,2.22(s,3H),2.00-1.57(m,16H),1.35-1.11(m,4H).
实施例48：1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基))))苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 48: 1-(2-Chloro-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-( (Dimethylamino)methyl))))phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-((1-(叔丁氧羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸苄酯的制备Step 1: Preparation of benzyl 4-(2-((1-(tert-butoxycarbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000893
Figure PCTCN2022088560-appb-000893
将化合物4-(2-羟基乙基)哌啶-1-羧酸苄酯(400mg,1.52mmol)溶于THF(5mL)中，加入三乙胺(230mg,2.28mmol)。将反应液冷却至0℃，滴加甲磺酰氯(208mg,1.82mmol)。滴加完毕，升温至室温反应2小时。加入氯化铵水溶液淬灭，乙酸乙酯(20mLx3)萃取，合并有几层并用饱和盐水洗涤，无水硫酸钠干燥，过滤浓缩得中间体。将此中间产物溶于四氢呋喃，加入到叔丁醇钾(340mg,3.04mmol)和化合物4-(羟基甲基)哌啶-1-羧酸叔丁酯(652mg,3.04mmol)的THF(6mL)溶液中，30℃下继续反应16小时。加入水稀释，用乙酸乙酯(20mLx3)萃取，合并有几层并用饱和盐水洗涤，无水硫酸钠干燥，过滤浓缩经柱层析(PE:EA＝5:1)纯化得到目标产物4-(2-((1-(叔丁氧羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸苄酯。The compound benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylate (400 mg, 1.52 mmol) was dissolved in THF (5 mL) and triethylamine (230 mg, 2.28 mmol) was added. The reaction solution was cooled to 0°C, and methanesulfonyl chloride (208 mg, 1.82 mmol) was added dropwise. After the dropwise addition was completed, the temperature was raised to room temperature to react for 2 hours. It was quenched by adding aqueous ammonium chloride solution, extracted with ethyl acetate (20 mL×3), several layers were combined and washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to obtain the intermediate. This intermediate was dissolved in tetrahydrofuran and added to potassium tert-butoxide (340 mg, 3.04 mmol) and compound 4-(hydroxymethyl)piperidine-1-carboxylate tert-butyl ester (652 mg, 3.04 mmol) in THF (6 mL) In the solution, the reaction was continued for 16 hours at 30°C. Add water to dilute, extract with ethyl acetate (20 mL×3), combine several layers and wash with saturated brine, dry over anhydrous sodium sulfate, filter and concentrate, and purify by column chromatography (PE:EA=5:1) to obtain the target product 4-( Benzyl 2-((1-(tert-butoxycarbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+Na] +＝483.2. LC-MS: (ESI, m/z): [M+Na] + = 483.2.
步骤2：4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000894
Figure PCTCN2022088560-appb-000894
将化合物4-(2-((1-(叔丁氧羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸苄酯溶于甲醇(180mg,0.39mmol)中，加入钯碳(70mg)。氢气(1个大气压)保护下置换三次，室温下继续反应16小时，硅藻土过滤，滤液浓缩得粗产品4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯，直接用于下一步。The compound benzyl 4-(2-((1-(tert-butoxycarbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carboxylate was dissolved in methanol (180 mg, 0.39 mmol) , and palladium on carbon (70 mg) was added. Replaced three times under the protection of hydrogen (1 atmosphere), continued the reaction for 16 hours at room temperature, filtered through celite, and concentrated the filtrate to obtain the crude product 4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine tert-butyl pyridine-1-carboxylate, used directly in the next step.
步骤3：4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯的制备Step 3: 4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl )thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy) Preparation of methyl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000895
Figure PCTCN2022088560-appb-000895
向化合物(1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹 唑啉-6-基)环己烷-1-羧酸(130mg,0.23mmol)的DMF(2mL)溶液中加入化合物4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯(114mg,0.35mmol)，TcFH(162mg,0.58mmol)和NMI(94mg,1.15mmol)，并于室温下反应16小时。反应完成后，反应液用水(20mL)淬灭并用乙酸乙酯(20mLx3)萃取。合并有机相并用盐水(50mL)洗涤，经硫酸钠干燥，过滤并真空浓缩。粗品通过柱层析纯化(NH 3/MeOH:DCM＝1:19～1:9)得到得目标产物4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯。 To compound (1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (130 mg, 0.23 mmol) in DMF (2 mL) was added compound 4-((2-( Piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate tert-butyl ester (114 mg, 0.35 mmol), TcFH (162 mg, 0.58 mmol) and NMI (94 mg, 1.15 mmol), and at room temperature The reaction was continued for 16 hours. After completion of the reaction, the reaction solution was quenched with water (20 mL) and extracted with ethyl acetate (20 mL×3). The organic phases were combined and washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by column chromatography (NH 3 /MeOH:DCM=1:19～1:9) to obtain the target product 4-((2-(1-((1R,4R)-4-(4-((( R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝867.3. LC-MS: (ESI, m/z): [M+H] + = 867.3.
步骤4：((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-基)甲酮的制备Step 4: ((1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1- The preparation of ketone
Figure PCTCN2022088560-appb-000896
Figure PCTCN2022088560-appb-000896
室温下将化合物4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羧酸叔丁酯(40mg,0.05mmol)溶于DCM(2mL)中，加入TFA(1mL)。室温下继续反应0.5小时。将反应液浓缩得到粗品((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-基)甲酮，无需进一步纯化直接用于下一步反应。Compound 4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)benzene yl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy )methyl)piperidine-1-carboxylate tert-butyl ester (40 mg, 0.05 mmol) was dissolved in DCM (2 mL) and TFA (1 mL) was added. The reaction was continued for 0.5 hours at room temperature. The reaction solution was concentrated to obtain crude product ((1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine -1-yl)methanone, which was used in the next reaction without further purification.
LC-MS:(ESI,m/z):[M+H] +＝767.3. LC-MS: (ESI, m/z): [M+H] + = 767.3.
步骤5：1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基))))苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(2-Chloro-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-(( Dimethylamino)methyl))))phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000897
Figure PCTCN2022088560-appb-000897
向((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-基)甲酮(50mg，0.07mmol)的DMSO(2mL)溶液中加入DIEA(103mg,0.80mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(42mg,0.10mmol)，并于室温下反应16小时。反应完成后，反应液用水(10mL)淬灭并用乙酸乙酯(10mLx3)萃取。合并有机相并用盐水(10mL)洗涤，经硫酸钠干燥，过滤并旋干。粗品通过制备纯化得到1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基))))苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。To ((1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(2-(piperidin-4-ylmethoxy)ethyl)piperidin-1-yl) To a solution of methyl ketone (50 mg, 0.07 mmol) in DMSO (2 mL) was added DIEA (103 mg, 0.80 mmol) and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzene Pentafluorophenyl formate (42 mg, 0.10 mmol) and reacted at room temperature for 16 hours. After completion of the reaction, the reaction solution was quenched with water (10 mL) and extracted with ethyl acetate (10 mL×3). The organic phases were combined and washed with brine (10 mL), dried over sodium sulfate, filtered and spin-dried. The crude product was purified by preparation to give 1-(2-chloro-5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2- ((dimethylamino)methyl))))phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1017.3. LC-MS: (ESI, m/z): [M+H] + = 1017.3.
1H NMR(400MHz,CD 3OD)δ7.99(s,1H),7.65-7.59(m,1H),7.52(s,1H),7.44-7.26(m,5H),7.24-7.16(m,2H),7.01(s,1H),6.11-6.01(m,1H),4.66-4.46(m,2H),4.09-3.98(m,1H),3.95(s,3H),3.81-3.67(m,3H),3.53-3.40(m,4H),3.16-3.00(m,3H),2.93-2.57(m,5H),2.52(s,3H),2.23-2.05(m,7H),1.95-1.57(m,15H),1.56-1.51(m,2H),1.34-1.00(m,7H). 1 H NMR (400MHz, CD 3 OD) δ 7.99(s, 1H), 7.65-7.59(m, 1H), 7.52(s, 1H), 7.44-7.26(m, 5H), 7.24-7.16(m, 2H), 7.01(s, 1H), 6.11-6.01(m, 1H), 4.66-4.46(m, 2H), 4.09-3.98(m, 1H), 3.95(s, 3H), 3.81-3.67(m, 3H), 3.53-3.40(m, 4H), 3.16-3.00(m, 3H), 2.93-2.57(m, 5H), 2.52(s, 3H), 2.23-2.05(m, 7H), 1.95-1.57( m,15H),1.56-1.51(m,2H),1.34-1.00(m,7H).
实施例49：(1R,4R)-N-(3-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基) 丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺Example 49: (1R,4R)-N-(3-(3-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3 -Azaspiro[5.5]undecan-9-yl)propyl)-4-(7-methoxy-2-methyl-4-(((R)-1-(4-(2-( (Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-carboxamide
步骤1：(E)-9-(3-乙氧基-3-氧代丙-1-烯-1-基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: (E)-tert-Butyl 9-(3-ethoxy-3-oxoprop-1-en-1-yl)-3-azaspiro[5.5]undecan-3-carboxylate preparation
Figure PCTCN2022088560-appb-000898
Figure PCTCN2022088560-appb-000898
0℃下，将NaH(214mg,5.33mmol,60％)加入到DMF(15mL)中，然后加入2-(二乙氧基磷酰基)乙酸乙酯(1.20g,5.33mmol)。0℃反应30分钟，加入9-甲酰基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.00g,3.55mmol)并在室温搅拌3h。反应结束，反应液冷却至0℃，加入NH 4Cl水溶液(100mL)稀释，并用乙酸乙酯(100mLx3)萃取。将合并的有机层用食盐水(100mL)洗涤，经硫酸钠干燥，过滤并减压浓缩，经层析柱(PE:EA＝0～1:4)纯化得到(E)-9-(3-乙氧基-3-氧代丙-1-烯-1-基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 At 0°C, NaH (214 mg, 5.33 mmol, 60%) was added to DMF (15 mL) followed by ethyl 2-(diethoxyphosphoryl)acetate (1.20 g, 5.33 mmol). The reaction was carried out at 0°C for 30 minutes, and 9-formyl-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (1.00 g, 3.55 mmol) was added and stirred at room temperature for 3 h. After the reaction was completed, the reaction solution was cooled to 0° C., diluted with aqueous NH 4 Cl solution (100 mL), and extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with brine (100 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure, and purified by column chromatography (PE:EA=0～1:4) to obtain (E)-9-(3- Ethoxy-3-oxoprop-1-en-1-yl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H-56] +＝296.2. LC-MS: (ESI, m/z): [M+H-56] + = 296.2.
步骤2：9-(3-乙氧基-3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-(3-ethoxy-3-oxopropyl)-3-azaspiro[5.5]undecane-3-carboxylate
Figure PCTCN2022088560-appb-000899
Figure PCTCN2022088560-appb-000899
将(E)-9-(3-乙氧基-3-氧代丙-1-烯-1-基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.1g,3.13mmol)的EtOH(20mL)溶液在H 2气氛和室温下加入Pd/C(150mg)并搅拌过夜。将混合物过滤并浓缩得到9-(3-乙氧基-3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 (E)-9-(3-ethoxy-3-oxoprop-1-en-1-yl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (1.1 g, 3.13 mmol) in EtOH (20 mL) was added Pd/C (150 mg) under H 2 atmosphere at room temperature and stirred overnight. The mixture was filtered and concentrated to give tert-butyl 9-(3-ethoxy-3-oxopropyl)-3-azaspiro[5.5]undecan-3-carboxylate.
LC-MS:(ESI,m/z):[M+H-56] +＝298.2. LC-MS: (ESI, m/z): [M+H-56] + = 298.2.
1H NMR(400MHz,CDCl 3)δ4.12(q,J＝7.2Hz,2H),3.40-3.30(m,4H),2.30(t,J＝7.6Hz,2H),1.71-1.62(m,2H),1.58-1.52(m,5H),1.47-1.42(m,10H),1.31-1.22(m,6H),1.13-1.02(m,4H). 1 H NMR (400 MHz, CDCl 3 ) δ 4.12 (q, J=7.2 Hz, 2H), 3.40-3.30 (m, 4H), 2.30 (t, J=7.6 Hz, 2H), 1.71-1.62 (m, 2H), 1.58-1.52(m, 5H), 1.47-1.42(m, 10H), 1.31-1.22(m, 6H), 1.13-1.02(m, 4H).
步骤3：9-(3-羟丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 9-(3-hydroxypropyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000900
Figure PCTCN2022088560-appb-000900
将9-(3-乙氧基-3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1g,2.83mmol)溶于THF(25mL)中，0℃下滴加LAH(3.4mmol,3.4mL,1M/THF)。在0℃下继续反应1h，然后加入Na 2SO 4.10H 2O淬灭，并搅拌20分钟以上。将混合物过滤，滤液浓缩得到9-(3-羟丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯，直接用于下一步反应。 9-(3-Ethoxy-3-oxopropyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (1 g, 2.83 mmol) was dissolved in THF (25 mL) , LAH (3.4mmol, 3.4mL, 1M/THF) was added dropwise at 0°C. The reaction was continued for 1 h at 0°C, then quenched by adding Na 2 SO 4 .10H 2 O, and stirring for more than 20 minutes. The mixture was filtered, and the filtrate was concentrated to obtain tert-butyl 9-(3-hydroxypropyl)-3-azaspiro[5.5]undecane-3-carboxylate, which was directly used in the next reaction.
1H NMR(400MHz,CDCl 3)δ3.63(t,J＝7.2Hz,2H),3.42-3.29(m,4H),1.69-1.53(m,6H),1.46-1.42(m,10H),1.32-1.22(m,6H),1.12-1.03(m,4H). 1 H NMR (400 MHz, CDCl 3 ) δ 3.63 (t, J=7.2 Hz, 2H), 3.42-3.29 (m, 4H), 1.69-1.53 (m, 6H), 1.46-1.42 (m, 10H), 1.32-1.22(m,6H),1.12-1.03(m,4H).
步骤4：9-(3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 9-(3-oxopropyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000901
Figure PCTCN2022088560-appb-000901
向9-(3-羟丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(850mg,2.7mmol)的DCM(25mL)溶液中分批加入戴斯-马丁氧化剂(1.37g，3.3mmol)。将混合物在室温搅拌1.5h。加入Na 2SO 3(50mL)和NaHCO 3(50mL) 水溶液淬灭，并用DCM(100mLx3)萃取。合并的有机层用无水硫酸钠干燥，过滤，滤液浓缩并通过硅胶柱层析(PE:EtOAc＝20:1～2:1)纯化得到9-(3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a solution of 9-(3-hydroxypropyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (850 mg, 2.7 mmol) in DCM (25 mL) was added Dess-Martin portionwise Oxidizing agent (1.37 g, 3.3 mmol). The mixture was stirred at room temperature for 1.5 h. It was quenched by adding aqueous Na2SO3 ( 50 mL) and NaHCO3 (50 mL) and extracted with DCM (100 mLx3 ). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated and purified by silica gel column chromatography (PE:EtOAc=20:1~2:1) to give 9-(3-oxopropyl)-3-nitrogen Heteraspiro[5.5]undecane-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H-100] +＝210.2. LC-MS: (ESI, m/z): [M+H-100] + = 210.2.
步骤5：9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 5: Preparation of tert-butyl 9-(3-((4-methoxybenzyl)(methyl)amino)propyl)-3-azaspiro[5.5]undecane-3-carboxylate
Figure PCTCN2022088560-appb-000902
Figure PCTCN2022088560-appb-000902
将9-(3-氧代丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(400mg,1.29mmol)和1-(4-甲氧基苯基)-N-甲基甲胺(0.39g,2.58mmol)溶于DCM/AcOH(25mL/0.5mL)中，室温搅拌1h。然后加入NaBH 3CN(162mg,2.58mmol)，室温反应16小时。反应液加入NH 4Cl水溶液(50mL)稀释，并用DCM(50mLx3)萃取。合并的有机层经硫酸钠干燥，过滤，滤液浓缩并经层析柱(DCM:MeOH＝200:1～5:1)纯化得到9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 9-(3-oxopropyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (400 mg, 1.29 mmol) and 1-(4-methoxyphenyl)- N-methylmethylamine (0.39 g, 2.58 mmol) was dissolved in DCM/AcOH (25 mL/0.5 mL) and stirred at room temperature for 1 h. Then NaBH 3 CN (162 mg, 2.58 mmol) was added and reacted at room temperature for 16 hours. The reaction solution was diluted with aqueous NH 4 Cl solution (50 mL), and extracted with DCM (50 mL×3). The combined organic layers were dried over sodium sulfate, filtered, and the filtrate was concentrated and purified by column chromatography (DCM:MeOH=200:1~5:1) to give 9-(3-((4-methoxybenzyl)(methyl) (yl)amino)propyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝445.4. LC-MS: (ESI, m/z): [M+H] + = 445.4.
步骤6：N-(4-甲氧基苄基)-N-甲基-3-(3-氮杂螺[5.5]十一烷-9-基)丙烷-1-胺的制备Step 6: Preparation of N-(4-Methoxybenzyl)-N-methyl-3-(3-azaspiro[5.5]undecan-9-yl)propan-1-amine
Figure PCTCN2022088560-appb-000903
Figure PCTCN2022088560-appb-000903
将9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(400mg,0.89mmol)溶于DCM(4.5mL)中，加入TFA(1.5mL)。反应液室温搅拌2h，浓缩得到N-(4-甲氧基苄基)-N-甲基-3-(3-氮杂螺[5.5]十一烷-9-基)丙烷-1-胺，直接用于下一步反应。9-(3-((4-Methoxybenzyl)(methyl)amino)propyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (400 mg, 0.89 mmol ) was dissolved in DCM (4.5 mL) and TFA (1.5 mL) was added. The reaction solution was stirred at room temperature for 2 h, and concentrated to obtain N-(4-methoxybenzyl)-N-methyl-3-(3-azaspiro[5.5]undecan-9-yl)propan-1-amine, used directly in the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝345.3. LC-MS: (ESI, m/z): [M+H] + = 345.3.
步骤7：1-(2-氯-5-(9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 7: 1-(2-Chloro-5-(9-(3-((4-methoxybenzyl)(methyl)amino)propyl)-3-azaspiro[5.5]undecane- Preparation of 3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000904
Figure PCTCN2022088560-appb-000904
向N-(4-甲氧基苄基)-N-甲基-3-(3-氮杂螺[5.5]十一烷-9-基)丙烷-1-胺(400mg,0.9mmol)的DMSO(2mL)溶液中加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸全五氟苯酯(470mg,1.08mmol)和DIEA(350mg,2.7mmol)。将反应液在室温搅拌2h。加入水(10mL)，并用EtOAc(20mLx2)萃取。合并有机层并用饱和盐水(50mLx3)洗涤，经无水硫酸钠干燥，过滤，滤液浓缩并经柱层析(DCM:MeOH＝200:1～5:1)纯化得到1-(2-氯-5-(9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。To N-(4-methoxybenzyl)-N-methyl-3-(3-azaspiro[5.5]undecan-9-yl)propan-1-amine (400 mg, 0.9 mmol) in DMSO (2 mL) solution was added perpentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (470 mg, 1.08 mmol) and DIEA (350 mg, 2.7 mmol). The reaction solution was stirred at room temperature for 2 h. Water (10 mL) was added and extracted with EtOAc (20 mL x 2). The organic layers were combined and washed with saturated brine (50 mL×3), dried over anhydrous sodium sulfate, filtered, the filtrate was concentrated and purified by column chromatography (DCM:MeOH=200:1~5:1) to give 1-(2-chloro-5). -(9-(3-((4-Methoxybenzyl)(methyl)amino)propyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine- 2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝595.2. LC-MS: (ESI, m/z): [M+H] + = 595.2.
步骤8：1-(2-氯-5-(9-(3-(甲基氨基)丙基)-3-)氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 8: 1-(2-Chloro-5-(9-(3-(methylamino)propyl)-3-)azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine Preparation of -2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000905
Figure PCTCN2022088560-appb-000905
将1-(2-氯-5-(9-(3-((4-甲氧基苄基)(甲基)氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(130mg,0.218mmol)和DIEA(14mg,0.11mmol)溶于DCM(3mL)中，0℃滴加氯甲酸2-氯乙酯(47mg,0.33mmol)。将混合物在室温下搅拌2h。然后加入MeOH(3mL)，在65℃下反应1h。将混合物浓缩并经柱层析(DCM:MeOH＝200:1～5:1)纯化得到1-(2-氯-5-(9-(3-(甲基氨基)丙基)-3-)氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(9-(3-((4-methoxybenzyl)(methyl)amino)propyl)-3-azaspiro[5.5]undecan-3- Carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (130 mg, 0.218 mmol) and DIEA (14 mg, 0.11 mmol) were dissolved in DCM (3 mL), and 2-chloroformic acid was added dropwise at 0°C Chloroethyl ester (47 mg, 0.33 mmol). The mixture was stirred at room temperature for 2 h. Then MeOH (3 mL) was added, and the reaction was carried out at 65° C. for 1 h. The mixture was concentrated and purified by column chromatography (DCM:MeOH=200:1~5:1) to give 1-(2-chloro-5-(9-(3-(methylamino)propyl)-3-) Azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝475.2. LC-MS: (ESI, m/z): [M+H] + = 475.2.
步骤9：(2-(5-((R)-1-((6-((1R,4R)-4-((3-(3-(4-氯-3-(2,4-二氧四氢嘧啶))-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)丙基)(甲基)氨基甲酰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基羧酸叔丁酯的制备Step 9: (2-(5-((R)-1-((6-((1R,4R)-4-((3-(3-(4-chloro-3-(2,4-dioxo) tetrahydropyrimidine))-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)propyl)(methyl)carbamoyl)cyclohexyl)-7 - Preparation of tert-butyl methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)aminocarboxylate
Figure PCTCN2022088560-appb-000906
Figure PCTCN2022088560-appb-000906
将1-(2-氯-5-(9-(3-(甲基氨基)丙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(100mg,0.21mmol)溶于DMSO(2mL)中，加入(1R,4R)-4-(4-(((R)-1-(4-(2-(((叔丁氧羰基)(甲基)氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸五氟苯酯(187mg,0.23mmol)和DIEA(82mg,0.63mmol)，室温下反应2h。反应结束，加入水(2mL)并用乙酸乙酯和水萃取。合并的有机层用硫酸钠干燥，过滤并浓缩，经层析柱(DCM:MeOH＝100:1～5:1)纯化得到目标化合物(2-(5-((R)-1-((6-((1R,4R)-4-((3-(3-(4-氯-3-(2,4-二氧四氢嘧啶))-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)丙基)(甲基)氨基甲酰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基羧酸叔丁酯。1-(2-Chloro-5-(9-(3-(methylamino)propyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2, 4(1H,3H)-dione (100 mg, 0.21 mmol) was dissolved in DMSO (2 mL), (1R,4R)-4-(4-(((R)-1-(4-(2-( ((tert-Butoxycarbonyl)(methyl)amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)ring Hexane-1-carboxylate pentafluorophenyl ester (187 mg, 0.23 mmol) and DIEA (82 mg, 0.63 mmol) were reacted at room temperature for 2 h. After the reaction was completed, water (2 mL) was added and extracted with ethyl acetate and water. The combined organic layers were dried over sodium sulfate, filtered and concentrated, and purified by column chromatography (DCM:MeOH=100:1～5:1) to give the title compound (2-(5-((R)-1-((6 -((1R,4R)-4-((3-(3-(4-chloro-3-(2,4-dioxotetrahydropyrimidine))-1(2H)-yl)benzoyl)-3 -Azaspiro[5.5]undecan-9-yl)propyl)(methyl)carbamoyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino) Ethyl)thiophen-3-yl)benzyl)(methyl)aminocarboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[1/2(M-100)+H] +＝501.2. LC-MS: (ESI, m/z): [1/2(M-100)+H] + =501.2.
步骤10：(1R,4R)-N-(3-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺的制备Step 10: (1R,4R)-N-(3-(3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3- Azaspiro[5.5]undecan-9-yl)propyl)-4-(7-methoxy-2-methyl-4-(((R)-1-(4-(2-(( Preparation of methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexane-1-carboxamide
Figure PCTCN2022088560-appb-000907
Figure PCTCN2022088560-appb-000907
化合物(2-(5-((R)-1-((6-((1R,4R)-4-((3-(3-(4-氯-3-(2,4-二氧四氢嘧啶))-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)丙基)(甲基)氨基甲酰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基羧酸叔丁酯(170mg,粗品)溶于DCM(4.5mL)，加入TFA(1.5mL)。将混合物在室温搅拌2h，浓缩并通过高效液相色谱制备纯化得到(1R,4R)-N-(3-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺 [5.5]十一烷-9-基)丙基)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)-N-甲基环己烷-1-甲酰胺。Compound (2-(5-((R)-1-((6-((1R,4R)-4-((3-(3-(4-chloro-3-(2,4-dioxotetrahydro) pyrimidine))-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)propyl)(methyl)carbamoyl)cyclohexyl)-7-methyl Oxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)aminocarboxylate (170 mg, crude) was dissolved in DCM (4.5 mL) ), TFA (1.5 mL) was added. The mixture was stirred at room temperature for 2 h, concentrated and purified by preparative high performance liquid chromatography to give (1R,4R)-N-(3-(3-(4-chloro-3-(2,4-dioxotetrahydropyrimidine)- 1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)propyl)-4-(7-methoxy-2-methyl-4-(( (R)-1-(4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)-N-methylcyclohexyl Alkane-1-carboxamide.
LC-MS:(ESI,m/z):[M+H] +＝1001.4. LC-MS: (ESI, m/z): [M+H] + = 1001.4.
1H NMR(400MHz,CD 3OD)δ8.02-7.96(m,1H),7.65-7.58(m,1H),7.54-7.48(m,1H),7.42-7.36(m,2H),7.32-7.26(m,3H),7.20-7.10(m,2H),7.01(s,1H),6.06(q,J＝6.8Hz,1H),3.95(s,3H),3.80-3.63(m,6H),3.48-3.34(m,4H),3.16-2.99(m,3H),2.93-2.82(m,3H),2.76-2.62(m,1H),2.52(s,3H),2.22(s,3H),2.03-1.85(m,4H),1.80-1.42(m,16H),1.37-1.15(m,8H). 1 H NMR (400MHz, CD 3 OD) δ 8.02-7.96 (m, 1H), 7.65-7.58 (m, 1H), 7.54-7.48 (m, 1H), 7.42-7.36 (m, 2H), 7.32- 7.26(m, 3H), 7.20-7.10(m, 2H), 7.01(s, 1H), 6.06(q, J=6.8Hz, 1H), 3.95(s, 3H), 3.80-3.63(m, 6H) ,3.48-3.34(m,4H),3.16-2.99(m,3H),2.93-2.82(m,3H),2.76-2.62(m,1H),2.52(s,3H),2.22(s,3H) ,2.03-1.85(m,4H),1.80-1.42(m,16H),1.37-1.15(m,8H).
实施例50：1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-))4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 50: 1-(2-Chloro-5-(9-(2-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-((((R)) -1-))4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidine Azin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-(2-乙氧基-2-氧代亚乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 9-(2-ethoxy-2-oxoethylene)-3-azaspiro[5.5]undecane-3-carboxylate
Figure PCTCN2022088560-appb-000908
Figure PCTCN2022088560-appb-000908
向搅拌的NaH(230mg,5.61mmol,60％)的DMF(15mL)溶液中加入2-(二乙氧基磷酰基)乙酸乙酯(1.26g,5.61mmol)。将混合物在0℃搅拌30分钟，然后加入9-氧代-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1g,3.74mmol)并在室温搅拌3h。混合物用NH 4Cl(100mL)水溶液，并用乙酸乙酯(100mLx3)萃取。将合并的有机层用盐水(100mL)洗涤，经硫酸钠干燥，过滤并减压浓缩，经柱层析纯化(EA:PE＝0～1:4)得到9-(2-乙氧基-2-氧代亚乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a stirred solution of NaH (230 mg, 5.61 mmol, 60%) in DMF (15 mL) was added ethyl 2-(diethoxyphosphoryl)acetate (1.26 g, 5.61 mmol). The mixture was stirred at 0°C for 30 minutes, then tert-butyl 9-oxo-3-azaspiro[5.5]undecan-3-carboxylate (1 g, 3.74 mmol) was added and stirred at room temperature for 3 h. The mixture was washed with aqueous NH4Cl (100 mL) and extracted with ethyl acetate (100 mL x 3). The combined organic layers were washed with brine (100 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure, and purified by column chromatography (EA:PE=0~1:4) to give 9-(2-ethoxy-2 -Oxoethylene)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝338.3. LC-MS: (ESI, m/z): [M+H] + = 338.3.
步骤2：9-(2-乙氧基-2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-(2-ethoxy-2-oxoethyl)-3-azaspiro[5.5]undecane-3-carboxylate
Figure PCTCN2022088560-appb-000909
Figure PCTCN2022088560-appb-000909
将9-(2-乙氧基-2-氧代亚乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1.1g,3.26mmol)溶于EtOH(20mL)中，在H 2氛围下搅拌过夜。将混合物过滤并浓缩得到9-(2-乙氧基-2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 9-(2-Ethoxy-2-oxoethylene)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (1.1 g, 3.26 mmol) was dissolved in EtOH (20 mL) ) , stirred under H atmosphere overnight. The mixture was filtered and concentrated to give tert-butyl 9-(2-ethoxy-2-oxoethyl)-3-azaspiro[5.5]undecan-3-carboxylate.
LC-MS:(ESI,m/z):[M+H-56] +＝284.2. LC-MS: (ESI, m/z): [M+H-56] + = 284.2.
步骤3：9-(2-羟基乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 9-(2-hydroxyethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000910
Figure PCTCN2022088560-appb-000910
搅拌下向9-(2-乙氧基-2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(1g,3mmol)的THF(25mL)溶液中加入LAH(3.6mmol,3.6mL,1M/THF)，在0℃至室温下反应1h。室温下向混合物中加入Na 2SO 4.10H 2O并搅拌1h以上。将混合物过滤并浓缩得到目标化合物9-(2-羟基乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a stirred solution of 9-(2-ethoxy-2-oxoethyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (1 g, 3 mmol) in THF (25 mL) LAH (3.6 mmol, 3.6 mL, 1M/THF) was added to it, and the reaction was carried out at 0°C to room temperature for 1 h. To the mixture was added Na2SO4.10H2O at room temperature and stirred for more than 1 h. The mixture was filtered and concentrated to give the target compound 9-(2-hydroxyethyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H-56] +＝242.2. LC-MS: (ESI, m/z): [M+H-56] + = 242.2.
步骤4：9-(2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 4: Preparation of tert-butyl 9-(2-oxoethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000911
Figure PCTCN2022088560-appb-000911
搅拌下向9-(2-羟基乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(850mg,2.5mmol)DCM(25mL)溶液中加入戴斯-马丁氧化剂(1.42g，3.6mmol)。将混合物在室温搅拌1.5h。混合物用Na 2SO 3(50mL)和NaHCO 3 (50mL)水溶液稀释，并用DCM(100mLx3)萃取。合并的有机层用硫酸钠干燥，过滤并减压浓缩，经柱层析(EA:PE＝0～3:2)纯化得到9-(2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a solution of 9-(2-hydroxyethyl)-3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (850 mg, 2.5 mmol) in DCM (25 mL) was added Dess-Martin oxidant with stirring (1.42 g, 3.6 mmol). The mixture was stirred at room temperature for 1.5 h. The mixture was diluted with aqueous Na2SO3 (50 mL) and NaHCO3 (50 mL) and extracted with DCM (100 mLx3 ). The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure, and purified by column chromatography (EA:PE=0～3:2) to obtain 9-(2-oxoethyl)-3-azaspiro[5.5 ] Undecane-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H-56] +＝240.2. LC-MS: (ESI, m/z): [M+H-56] + = 240.2.
步骤5：9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 5: tert-butyl 9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carboxylate preparation
Figure PCTCN2022088560-appb-000912
Figure PCTCN2022088560-appb-000912
搅拌下向9-(2-氧代乙基)-3-氮杂螺[5.5]十一烷-3-甲酸叔丁酯(750mg,2.54mmol)的DCM/HAc(25mL/0.5mL)溶液中加入1-(4-甲氧基苄基)哌嗪(0.79g,3.81mmol)。将混合物在室温搅拌1h。然后加入NaBH 3CN(320mg,5.08mmol)。混合物用NH 4Cl(50mL)水溶液稀释，并用DCM(50mLx3)萃取。合并的有机层用硫酸钠干燥，过滤并减压浓缩，经柱层析(DCM:MeOH＝0～1:4)纯化得到9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 To a stirred solution of tert-butyl 9-(2-oxoethyl)-3-azaspiro[5.5]undecane-3-carboxylate (750 mg, 2.54 mmol) in DCM/HAc (25 mL/0.5 mL) 1-(4-Methoxybenzyl)piperazine (0.79 g, 3.81 mmol) was added. The mixture was stirred at room temperature for 1 h. Then NaBH3CN (320 mg, 5.08 mmol) was added. The mixture was diluted with aqueous NH4Cl (50 mL) and extracted with DCM (50 mL x 3). The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure, and purified by column chromatography (DCM:MeOH=0~1:4) to give 9-(2-(4-(4-methoxybenzyl)piperidine) oxazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝486.4. LC-MS: (ESI, m/z): [M+H] + = 486.4.
步骤6：9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷的制备Step 6: Preparation of 9-(2-(4-(4-Methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecane
Figure PCTCN2022088560-appb-000913
Figure PCTCN2022088560-appb-000913
搅拌下向9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(100mg,0.21mmol)的DCM(1.5mL)溶液中滴加TFA(0.5mL)。将混合物在室温搅拌2h，反应液减压浓缩得到9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷。To tert-butyl 9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carboxylate with stirring (100 mg, 0.21 mmol) in DCM (1.5 mL) was added dropwise TFA (0.5 mL). The mixture was stirred at room temperature for 2 h, and the reaction solution was concentrated under reduced pressure to obtain 9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]ten an alkane.
LC-MS:(ESI,m/z):[M+H] +＝386.4. LC-MS: (ESI, m/z): [M+H] + = 386.4.
步骤7：1-(2-氯-5-(9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Step 7: 1-(2-Chloro-5-(9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]dec Monoalkane-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000914
Figure PCTCN2022088560-appb-000914
向9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷(100mg,粗品)在DMSO(2mL)中的搅拌溶液中加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(99mg,0.23mmol)和DIEA(80mg,0.62mmol)。将混合物在室温搅拌2h并用EA和水萃取。合并的有机层经硫酸钠干燥，过滤并减压浓缩，经柱层析(DCM:MeOH＝0～1:4)纯化得到1-(2-氯-5-(9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。To 9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecane (100 mg, crude) in DMSO (2 mL) To the stirred solution in , was added pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (99 mg, 0.23 mmol) and DIEA (80 mg, 0.62 mmol) ). The mixture was stirred at room temperature for 2 h and extracted with EA and water. The combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure, and purified by column chromatography (DCM:MeOH=0~1:4) to give 1-(2-chloro-5-(9-(2-(4- (4-Methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H )-diketone.
LC-MS:(ESI,m/z):[M+H] +＝636.4. LC-MS: (ESI, m/z): [M+H] + = 636.4.
步骤8：1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)))-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 8: 1-(2-Chloro-5-(9-(2-(piperazin-1-yl)ethyl)))-3-azaspiro[5.5]undecan-3-carbonyl)phenyl ) Preparation of dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000915
Figure PCTCN2022088560-appb-000915
将1-(2-氯-5-(9-(2-(4-(4-甲氧基苄基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(90mg,0.14mmol)溶于DCM(2mL)中，加入氯甲酸2-氯乙酯(30mg,0.22mmol)和DIEA(9mg,0.071mmol)。将混合物在0℃至室温下搅拌2h。然后在65℃下再加入MeOH(3mL)并继续搅拌1h。将混合物浓缩并经柱层析(DCM:MeOH＝0～1:4)纯化得到1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)))-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(9-(2-(4-(4-methoxybenzyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecane -3-Carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (90 mg, 0.14 mmol) was dissolved in DCM (2 mL) and 2-chloroethyl chloroformate (30 mg, 0.22 mmol) was added ) and DIEA (9 mg, 0.071 mmol). The mixture was stirred at 0 °C to room temperature for 2 h. Additional MeOH (3 mL) was then added at 65°C and stirring was continued for 1 h. The mixture was concentrated and purified by column chromatography (DCM:MeOH=0~1:4) to give 1-(2-chloro-5-(9-(2-(piperazin-1-yl)ethyl)))- 3-Azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝516.3. LC-MS: (ESI, m/z): [M+H] + = 516.3.
步骤9：(2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基羧酸叔丁酯的制备Step 9: (2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4-chloro-3-(2,4- Dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)ethyl)piperazine-1-carbonyl)cyclohexyl)-7 - Preparation of tert-butyl methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)aminocarboxylate
Figure PCTCN2022088560-appb-000916
Figure PCTCN2022088560-appb-000916
将1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(63mg,0.12mmol)溶于DMSO(2mL)中，加入(1R,4R)-4-(4-(((R)-1-(4-(2-(((叔丁氧基羰基)(甲基)氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸五氟苯酯(109mg,0.13mmol)和DIEA(48mg,0.36mmol)。将混合物在室温搅拌2h并用EA和水萃取。合并的有机层用硫酸钠干燥，过滤并浓缩得到(2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基羧酸叔丁酯。1-(2-Chloro-5-(9-(2-(piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine -2,4(1H,3H)-dione (63 mg, 0.12 mmol) was dissolved in DMSO (2 mL), (1R,4R)-4-(4-(((R)-1-(4-( 2-(((tert-butoxycarbonyl)(methyl)amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6 -yl)cyclohexane-1-carboxylate pentafluorophenyl ester (109 mg, 0.13 mmol) and DIEA (48 mg, 0.36 mmol). The mixture was stirred at room temperature for 2 h and extracted with EA and water. The combined organic layers were dried over sodium sulfate, filtered and concentrated to give (2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4 -Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)ethyl)piperazine -1-Carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)aminocarboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[(M-56)/2+H]+＝544.3.LC-MS: (ESI, m/z): [(M-56)/2+H]+=544.3.
步骤10：1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-))4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 10: 1-(2-Chloro-5-(9-(2-(4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)- 1-))4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine Preparation of -1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000917
Figure PCTCN2022088560-appb-000917
将(2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰基)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)氨基甲羧酸叔丁酯(160mg,粗品)溶于DCM(4.5mL)中，加入TFA(1.5mL)。将混合物在室温搅拌2h，浓缩并通过制备纯化得到1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-))4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。(2-(5-((R)-1-((6-((1R,4R)-4-(4-(2-(3-(4-chloro-3-(2,4-dioxo) tetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)ethyl)piperazine-1-carbonyl)cyclohexyl)-7-methyl Oxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carbamic acid tert-butyl ester (160 mg, crude) was dissolved in DCM (4.5 mL), TFA (1.5 mL) was added. The mixture was stirred at room temperature for 2 h, concentrated and purified by prep to give 1-(2-chloro-5-(9-(2-(4-((1R,4R)-4-(7-methoxy-2-methyl) base-4-(((R)-1-))4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl) Cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H) - Diketones.
LC-MS:(ESI,m/z):[M+H] +＝1042.4. LC-MS: (ESI, m/z): [M+H] + = 1042.4.
1H NMR(400MHz,CD 3OD)δ7.98(s,1H),7.68-7.56(m,1H),7.57-7.48(m,1H),7.45-7.35(m,2H),7.34-7.24(m,3H),7.22-7.10(m,2H),7.01(s,1H),6.06(q,J＝6.9Hz,1H),3.95(s,3H),3.83-3.73(m,2H),3.74-3.68(m,3H),3.66-3.55(m,4H),3.45-3.34(m,2H),3.12-3.01(m,1H),2.93-2.76(m,2H),2.76-2.66(m,1H),2.55-2.39(m,8H),2.21(s,3H),2.03-1.86(m,4H),1.81-1.75(m,4H),1.70-1.57(m,6H),1.45-1.16(m,14H). 1 H NMR (400MHz, CD 3 OD) δ 7.98(s, 1H), 7.68-7.56(m, 1H), 7.57-7.48(m, 1H), 7.45-7.35(m, 2H), 7.34-7.24( m,3H),7.22-7.10(m,2H),7.01(s,1H),6.06(q,J=6.9Hz,1H),3.95(s,3H),3.83-3.73(m,2H),3.74 -3.68(m, 3H), 3.66-3.55(m, 4H), 3.45-3.34(m, 2H), 3.12-3.01(m, 1H), 2.93-2.76(m, 2H), 2.76-2.66(m, 1H), 2.55-2.39(m, 8H), 2.21(s, 3H), 2.03-1.86(m, 4H), 1.81-1.75(m, 4H), 1.70-1.57(m, 6H), 1.45-1.16( m,14H).
实施例51：1-(5-(9-((4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 51: 1-(5-(9-((4-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino )-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-((4-(叔丁氧羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的制备Step 1: Preparation of benzyl 9-((4-(tert-butoxycarbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000918
Figure PCTCN2022088560-appb-000918
将9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(400mg,1.04mmol)用DCM(10mL)溶解，分别加入(Boc) 2O(272mg,1.25mmol)，DMAP(13mg,0.1mmol)和TEA(315mg,3.12mmol)，反应液室温下搅拌过夜，直接减压浓缩。粗品使用柱层析(PE:EA＝1:1)纯化得到9-((4-(叔丁氧羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯。 Benzyl 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate (400 mg, 1.04 mmol) was dissolved in DCM (10 mL) and (Boc) was added separately 2 O (272 mg, 1.25 mmol), DMAP (13 mg, 0.1 mmol) and TEA (315 mg, 3.12 mmol), the reaction solution was stirred at room temperature overnight, and directly concentrated under reduced pressure. The crude product was purified using column chromatography (PE:EA=1:1) to give 9-((4-(tert-butoxycarbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecane - Benzyl 3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝486.3. LC-MS: (ESI, m/z): [M+H] + = 486.3.
步骤2：4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000919
Figure PCTCN2022088560-appb-000919
将9-((4-(叔丁氧羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(300mg,0.62mmol)用乙酸乙酯(10mL)溶解，加入Pd(OH) 2/C(100mg)，反应液70℃下搅拌3小时，冷却，过滤，固体用乙酸乙酯(10mL×3)洗三次，减压浓缩，得到粗品4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯。 Benzyl 9-((4-(tert-butoxycarbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate (300 mg, 0.62 mmol) was treated with acetic acid Ethyl ester (10 mL) was dissolved, Pd(OH) 2 /C (100 mg) was added, the reaction solution was stirred at 70° C. for 3 hours, cooled, filtered, the solid was washed three times with ethyl acetate (10 mL×3), and concentrated under reduced pressure to obtain Crude tert-butyl 4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝352.2. LC-MS: (ESI, m/z): [M+H] + = 352.2.
步骤3：4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯的制备Step 3: 4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane Preparation of tert-butyl alkane-9-yl)methyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000920
Figure PCTCN2022088560-appb-000920
将4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯(200mg,0.57mmol)用DMSO(10mL)溶解，加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-yl)苯甲酸五氟苯酯(247mg,0.57mmol)和DIEA(220mg,1.71mmol)，反应液室温下搅拌2小时，加入水(50mL)，用乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝1:10)纯化得到4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯。4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylate tert-butyl ester (200 mg, 0.57 mmol) was dissolved in DMSO (10 mL), 4- Chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)-yl)pentafluorophenyl benzoate (247mg, 0.57mmol) and DIEA (220mg, 1.71mmol), the reaction solution was stirred at room temperature for 2 hour, water (50 mL) was added, extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:10) to obtain 4 -((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9- yl)methyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝602.2. LC-MS: (ESI, m/z): [M+H] + = 602.2.
步骤4：1-(2-氯-5-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(2-Chloro-5-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2 Preparation of ,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000921
Figure PCTCN2022088560-appb-000921
将4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸叔丁酯(350mg,0.58mmol)用DCM(5mL)溶解，加入TFA(1mL)，然后反应液室温搅拌2小时，减压浓缩，残余物用水(20mL)稀释，缓慢滴加饱和碳酸氢钠溶液将反应液调至中性，用乙酸乙酯(25mL×4)萃取， 饱和食盐水洗，无水硫酸钠干燥，减压浓缩得到粗品1-(2-氯-5-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane- 9-yl)methyl)piperazine-1-carboxylate tert-butyl ester (350 mg, 0.58 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, the reaction solution was stirred at room temperature for 2 hours, concentrated under reduced pressure, and the residue was It was diluted with water (20 mL), and saturated sodium bicarbonate solution was slowly added dropwise to make the reaction solution neutral, extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the crude product 1- (2-Chloro-5-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H, 3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝502.3. LC-MS: (ESI, m/z): [M+H] + = 502.3.
步骤5：(3-((1R)-1-((6-(4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 5: (3-((1R)-1-((6-(4-(4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)) -yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexane-1-yl)-7-methoxy-2 - Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000922
Figure PCTCN2022088560-appb-000922
将1-(2-氯-5-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(125mg,0.25mmol)用DMF(10mL)溶解，分别加入4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸(140mg,0.23mmol)，HATU(114mg,0.30mmol)和DIEA(129mg,1.00mmol)，反应液室温搅拌2小时，加入水(100mL)，析出固体，过滤，水洗3次，用二氯甲烷溶解，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:10)纯化得到(3-((1R)-1-((6-(4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。1-(2-Chloro-5-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4 (1H,3H)-dione (125 mg, 0.25 mmol) was dissolved in DMF (10 mL), and 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5 -(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid (140 mg, 0.23 mmol ), HATU (114 mg, 0.30 mmol) and DIEA (129 mg, 1.00 mmol), the reaction solution was stirred at room temperature for 2 hours, water (100 mL) was added, a solid was precipitated, filtered, washed with water 3 times, dissolved in dichloromethane, anhydrous sodium sulfate It was dried, concentrated under reduced pressure, and the crude product was purified by column chromatography (MeOH:DCM=1:10) to give (3-((1R)-1-((6-(4-(4-((3-(4-chloro) -3-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1 -Carbonyl)cyclohexane-1-yl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylic acid tert. Butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1095.5. LC-MS: (ESI, m/z): [M+H] + = 1095.5.
步骤6：1-(5-(9-((4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(9-((4-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]dec Preparation of monoalkane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000923
Figure PCTCN2022088560-appb-000923
将(3-((1R)-1-((6-(4-(4-((3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(100mg,0.09mmol)用DCM(5mL)溶解，加入TFA(1mL)，然后反应液室温搅拌过夜，减压浓缩，用水(20mL)稀释，缓慢滴加碳酸氢钠溶液将反应液调至中性，用二氯甲烷(25mL×4)萃取，无水硫酸钠干燥，减压浓缩，粗品使用反相制备纯化得到1-(5-(9-((4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((1R)-1-((6-(4-(4-((3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) )benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexane-1-yl)-7-methoxy-2-methyl tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (100 mg, 0.09 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, Then the reaction solution was stirred at room temperature overnight, concentrated under reduced pressure, diluted with water (20 mL), slowly added dropwise with sodium bicarbonate solution to make the reaction solution neutral, extracted with dichloromethane (25 mL×4), dried over anhydrous sodium sulfate, reduced was concentrated under pressure, and the crude product was purified by reverse-phase preparation to give 1-(5-(9-((4-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene)) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperazin-1-yl)methyl)-3- Azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝984.3. LC-MS: (ESI, m/z): [M+H] + = 984.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.18(s,1H),8.06(s,1H),7.63(d,J＝8.2Hz,1H),7.55(d,J＝1.7Hz,1H),7.39(d,J＝8.3Hz,1H),6.99(s,1H),6.89(s,1H),6.85(s,1H),6.69(s,1H),5.83(s,1H),5.59-5.47(m,3H),3.85(s,3H),3.80-3.70(m,1H),3.67-3.45(m,7H),2.94-2.82(m,1H),2.77-2.71(m,2H),,2.42-2.10(m,13H),1.89-1.81(m,1H),1.73-1.25(m,15H),1.18-0.94(m,4H). 1H NMR (400MHz, DMSO-d 6 )δ10.50(s,1H), 8.18(s,1H), 8.06(s,1H), 7.63(d,J=8.2Hz,1H), 7.55(d,J) =1.7Hz,1H),7.39(d,J=8.3Hz,1H),6.99(s,1H),6.89(s,1H),6.85(s,1H),6.69(s,1H),5.83(s ,1H),5.59-5.47(m,3H),3.85(s,3H),3.80-3.70(m,1H),3.67-3.45(m,7H),2.94-2.82(m,1H),2.77-2.71 (m,2H),,2.42-2.10(m,13H),1.89-1.81(m,1H),1.73-1.25(m,15H),1.18-0.94(m,4H).
实施例52：3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮Example 52: 3-(4-(9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) (ylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione
步骤1：9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: 9-((4-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 - Preparation of tert-butyl carboxylate
Figure PCTCN2022088560-appb-000924
Figure PCTCN2022088560-appb-000924
将9-醛-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(200mg,0.71mmol)溶于四氢呋喃(4mL)溶液中，加入哌 嗪-1-羧酸(9H-芴-9-基)甲基酯(219mg,0.71mmol)和三乙酰氧基硼氢化钠(449mg,2.13mmol)，反应液在常温下搅拌过夜，用水(40mL)稀释，乙酸乙酯(80mL×2)萃取，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(乙酸乙酯:石油醚＝1:1)纯化得到9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。9-Al-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester (200 mg, 0.71 mmol) was dissolved in tetrahydrofuran (4 mL) solution, piperazine-1-carboxylic acid (9H- Fluoren-9-yl)methyl ester (219mg, 0.71mmol) and sodium triacetoxyborohydride (449mg, 2.13mmol), the reaction solution was stirred at room temperature overnight, diluted with water (40mL), ethyl acetate (80mL× 2) Extraction, drying over anhydrous sodium sulfate, filtration, concentration under reduced pressure, and the crude product was purified by column chromatography (ethyl acetate:petroleum ether=1:1) to obtain 9-((4-(((9H-fluorene-9- yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝574.4. LC-MS: (ESI, m/z): [M+H] + = 574.4.
步骤2：4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯的制备Step 2: Preparation of 4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester
Figure PCTCN2022088560-appb-000925
Figure PCTCN2022088560-appb-000925
将9-((4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(400mg,0.7mmol)溶于氯化氢的1,4-二氧六环(4mmol/L,5mL)溶液中，反应液在室温下搅拌1小时，直接减压浓缩得到4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯。9-((4-(((9H-fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxy Acid tert-butyl ester (400 mg, 0.7 mmol) was dissolved in a solution of hydrogen chloride in 1,4-dioxane (4 mmol/L, 5 mL), the reaction solution was stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain 4-(( 3-Azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝474.5. LC-MS: (ESI, m/z): [M+H] + = 474.5.
步骤3：4-((3-(4-(2,6-二氧代哌啶-3-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯的制备Step 3: 4-((3-(4-(2,6-dioxopiperidin-3-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl ) Preparation of piperazine-1-carboxylic acid (9H-fluoren-9-yl) methyl ester
Figure PCTCN2022088560-appb-000926
Figure PCTCN2022088560-appb-000926
将4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯(340mg,0.72mmol)用DMSO(4mL)溶解，4-(2,6-二氧代哌啶-3-基)苯甲酸五氟苯酯(287mg，0.72mmol)和DIEA(371mg,2.87mmol)加入，反应液在室温下搅拌过夜，用水(40mL)稀释，乙酸乙酯(40mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝1:2)纯化得到4-((3-(4-(2,6-二氧代哌啶-3-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯。4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester (340 mg, 0.72 mmol) was used DMSO (4 mL) was dissolved, 4-(2,6-dioxopiperidin-3-yl) benzoic acid pentafluorophenyl ester (287 mg, 0.72 mmol) and DIEA (371 mg, 2.87 mmol) were added, the reaction solution was at room temperature Stir overnight, diluted with water (40 mL), extracted with ethyl acetate (40 mL×3), the organic phase was washed with saturated brine (40 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was subjected to column chromatography (PE:EA= 1:2) Purification to give 4-((3-(4-(2,6-dioxopiperidin-3-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl ) methyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝689.5. LC-MS: (ESI, m/z): [M+H] + = 689.5.
步骤4：3-(4-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮的制备Step 4: 3-(4-(9-(Piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione preparation
Figure PCTCN2022088560-appb-000927
Figure PCTCN2022088560-appb-000927
将4-((3-(4-(2,6-二氧代哌啶-3-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羧酸(9H-芴-9-基)甲基酯(250mg,0.36mmol)用二氯甲烷(4mL)溶解，然后加入哌啶(0.25mL)，反应液在室温搅拌3小时，直接解压浓缩得到3-(4-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮。4-((3-(4-(2,6-dioxopiperidin-3-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperidine Azine-1-carboxylic acid (9H-fluoren-9-yl) methyl ester (250 mg, 0.36 mmol) was dissolved in dichloromethane (4 mL), then piperidine (0.25 mL) was added, and the reaction solution was stirred at room temperature for 3 hours, Direct decompression and concentration to obtain 3-(4-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-di ketone.
LC-MS:(ESI,m/z):[M+H] +＝467.4. LC-MS: (ESI, m/z): [M+H] + = 467.4.
步骤5：3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮的制备Step 5: 3-(4-(9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) Amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1 Preparation of -yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione
Figure PCTCN2022088560-appb-000928
Figure PCTCN2022088560-appb-000928
将3-(4-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮(200mg,0.43mmol)用DMF(3mL)溶解，(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(254mg,0.43mmol)，HATU(196mg,0.52mmol)和DIEA(221mg,1.7mmol)分别加入，反应液室温搅拌3小时，用水(40mL)稀释，乙酸乙酯(40mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用Prep-HPLC纯化得到3-(4-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)哌啶-2,6-二酮。3-(4-(9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione (200 mg , 0.43 mmol) was dissolved in DMF (3 mL), (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) Phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (254 mg, 0.43 mmol), HATU ( 196 mg, 0.52 mmol) and DIEA (221 mg, 1.7 mmol) were added respectively, the reaction solution was stirred at room temperature for 3 hours, diluted with water (40 mL), extracted with ethyl acetate (40 mL×3), and the organic phase was washed with saturated brine (40 mL), It was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by Prep-HPLC to obtain 3-(4-(9-((4-((1R,4R)-4-(4-((((R)-1-() 4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6- yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)piperidine-2,6-dione.
LC-MS:(ESI,m/z):[M+H] +＝1041.6. LC-MS: (ESI, m/z): [M+H] + = 1041.6.
1H NMR(400MHz,DMSO-d 6)δ10.86(s,1H),8.31(d,J＝8.5Hz,1H),8.05(s,1H),7.45–7.40(s,2H),7.36–7.32(s,3H),7.28(d,J＝8.1Hz,2H),7.24(d,J＝1.2Hz,1H),7.01(s,1H),6.96(s,1H),5.99–5.94(m,1H),3.94–3.87(m,4H),3.57(s,2H),3.46(s,5H),3.12(s,2H),2.94(s,1H),2.74–2.59(m,4H),2.42(s,3H),2.23(d,J＝13.2Hz,5H),2.17–2.04(m,4H),2.01(s,7H),1.88–1.76(m,5H),1.71(d,J＝6.9Hz,4H),1.68(s,1H),1.64–1.48(m,8H),1.23(s,2H),1.07(s,3H). 1H NMR (400MHz, DMSO-d 6 ) δ 10.86(s, 1H), 8.31(d, J=8.5Hz, 1H), 8.05(s, 1H), 7.45-7.40(s, 2H), 7.36-7.32 (s, 3H), 7.28(d, J=8.1Hz, 2H), 7.24(d, J=1.2Hz, 1H), 7.01(s, 1H), 6.96(s, 1H), 5.99–5.94(m, 1H), 3.94–3.87(m, 4H), 3.57(s, 2H), 3.46(s, 5H), 3.12(s, 2H), 2.94(s, 1H), 2.74–2.59(m, 4H), 2.42 (s, 3H), 2.23 (d, J=13.2Hz, 5H), 2.17–2.04 (m, 4H), 2.01 (s, 7H), 1.88–1.76 (m, 5H), 1.71 (d, J=6.9 Hz, 4H), 1.68(s, 1H), 1.64–1.48(m, 8H), 1.23(s, 2H), 1.07(s, 3H).
实施例53：1-(5-(4-((2-(4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 53: 1-(5-(4-((2-(4-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperazin-1-yl)ethoxy)methyl)piperidine -1-Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯的制备Step 1: 4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methan Preparation of tert-butyl oxy)ethyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000929
Figure PCTCN2022088560-appb-000929
将4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(140mg,0.32mmol)用DMSO(5mL)溶解，加入4-(2-(哌啶-4-基甲氧基)乙基)哌嗪-1-羧酸叔丁酯(116mg,0.35mmol)和DIEA(124mg,0.96mmol)，室温搅拌2小时，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯。Pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (140 mg, 0.32 mmol) was dissolved in DMSO (5 mL), 4-(2 -(Piperidin-4-ylmethoxy)ethyl)piperazine-1-carboxylate tert-butyl ester (116 mg, 0.35 mmol) and DIEA (124 mg, 0.96 mmol), stirred at room temperature for 2 hours, added water (50 mL) and Stirred for 5 minutes, extracted with ethyl acetate (30 mL×3), washed the organic phase with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (MeOH:DCM=1:9) Purification to give 4-(2-((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy yl)ethyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝578.2. LC-MS: (ESI, m/z): [M+H] + = 578.2.
步骤2：1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2, Preparation of 4(1H,3H)-dione
Figure PCTCN2022088560-appb-000930
Figure PCTCN2022088560-appb-000930
将4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羧酸叔丁酯(170mg,0.29mmol)溶于DCM(5mL)中，加入TFA(1mL)，室温搅拌2小时，减压浓缩得到1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，直接用于下一步。4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy )ethyl)piperazine-1-carboxylate tert-butyl ester (170 mg, 0.29 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, stirred at room temperature for 2 hours, and concentrated under reduced pressure to give 1-(2-chloro- 5-(4-((2-(Piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione, used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝478.2. LC-MS: (ESI, m/z): [M+H] + = 478.2.
步骤3：(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙 基)哌嗪-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)本家)羧酸叔丁酯的制备Step 3: (3-((1R)-1-((6-(4-(4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine-1 (2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2 - Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)honji)carboxylate
Figure PCTCN2022088560-appb-000931
Figure PCTCN2022088560-appb-000931
将1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(170mg，0.36mmol)溶于DMF(5mL)，加入4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸(150mg,0.25mmol)，HATU(124mg,0.32mmol)和DIEA(161mg,1.25mmol)，室温搅拌2小时，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)提取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)本家)羧酸叔丁酯。1-(2-Chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione (170 mg, 0.36 mmol) was dissolved in DMF (5 mL), 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-( trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid (150 mg, 0.25 mmol), HATU (124 mg, 0.32 mmol) and DIEA (161 mg, 1.25 mmol) were stirred at room temperature for 2 hours, water (50 mL) was added and stirred for 5 minutes, extracted with ethyl acetate (30 mL×3), and the organic phase was washed with saturated brine (50 mL). Dry over anhydrous sodium sulfate, filter, and concentrate under reduced pressure. The crude product was purified by column chromatography (MeOH:DCM=1:9) to give (3-((1R)-1-((6-(4-(4-(2). -((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine oxazine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl) Home) tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝1060.4. LC-MS: (ESI, m/z): [M+H] + = 1060.4.
步骤4：1-(5-(4-((2-(4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(5-(4-((2-(4-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperazin-1-yl)ethoxy)methyl)piperidine- Preparation of 1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000932
Figure PCTCN2022088560-appb-000932
将(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌嗪-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)本家)羧酸叔丁酯(140mg，0.13mmol)溶于DCM(5mL)中，加入TFA(1mL)，室温搅拌2小时，减压浓缩后，加入MeOH/DCM(1/9,20mL)溶解，再加入饱和碳酸氢钠水溶液(20mL)调节pH至中性，搅拌10分钟后，用MeOH/DCM(1/9,20mL×3)提取，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(4-((2-(4-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((1R)-1-((6-(4-(4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H )-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperazine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2-methyl (140 mg, 0.13 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, The mixture was stirred at room temperature for 2 hours, concentrated under reduced pressure, dissolved in MeOH/DCM (1/9, 20 mL), and then added with saturated aqueous sodium bicarbonate solution (20 mL) to adjust the pH to neutral. /9, 20mL×3) extraction, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was purified by reverse-phase preparation to obtain 1-(5-(4-((2-(4-(4-(4- (((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl -3-En-1-carbonyl)piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)- diketone.
LC-MS:(ESI,m/z):[M+H] +＝960.4. LC-MS: (ESI, m/z): [M+H] + = 960.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.18(d,J＝7.8Hz,1H),8.06(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝2.0Hz,1H),7.38(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.69(s,1H),5.83(s,1H),5.55–5.45(m,3H),4.50-4.36(m,1H),3.85(s,3H),3.75(d,J＝7.2Hz,1H),3.67–3.37(m,9H),3.06(s,1H),2.87(s,1H),2.81–2.69(m,3H),2.47–2.16(m,13H),1.89–1.41(m,9H),1.20–1.13(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.18(d, J=7.8Hz, 1H), 8.06(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝2.0Hz,1H),7.38(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.88(s,1H),6.85(s,1H),6.69( s, 1H), 5.83(s, 1H), 5.55-5.45(m, 3H), 4.50-4.36(m, 1H), 3.85(s, 3H), 3.75(d, J=7.2Hz, 1H), 3.67 –3.37(m, 9H), 3.06(s, 1H), 2.87(s, 1H), 2.81 – 2.69(m, 3H), 2.47 – 2.16(m, 13H), 1.89 – 1.41(m, 9H), 1.20 –1.13(m,2H).
实施例54：1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 54: 1-(2-Chloro-5-(4-(3-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(对甲苯磺酰)丙基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(3-(p-toluenesulfonyl)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000933
Figure PCTCN2022088560-appb-000933
将4-(3-羟基丙基)哌啶-1-羧酸叔丁酯(3.6g,14.81mmol)用二氯甲烷(20mL)溶解，分别加入TsCl(3.4g,17.80mmol)，DMAP(180mg,1.48mmol)和TEA(4.5g,44.43mmol)，反应液室温搅拌过夜，反应液直接减压浓缩，粗品经柱层析(PE:EA＝5:1)纯化得到4-(3-(对甲苯磺酰)丙基)哌啶-1-羧酸叔丁酯。Dissolve 4-(3-hydroxypropyl)piperidine-1-carboxylate tert-butyl ester (3.6g, 14.81mmol) in dichloromethane (20mL), add TsCl (3.4g, 17.80mmol), DMAP (180mg) respectively , 1.48 mmol) and TEA (4.5 g, 44.43 mmol), the reaction solution was stirred at room temperature overnight, the reaction solution was directly concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=5:1) to obtain 4-(3-(to) Tosyl)propyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝398.1. LC-MS: (ESI, m/z): [M+H] + = 398.1.
步骤2：4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙氧基)哌啶-1-羧酸苄酯的制备Step 2: Preparation of benzyl 4-(3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propoxy)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000934
Figure PCTCN2022088560-appb-000934
将4-羟基哌啶-1-羧酸苄酯(4.4g,18.51mmol)用无水DMF(10mL)溶解并冷却到0℃，加入NaH(0.6g,24.68mmol)，搅拌0.5小时，然后室温搅拌1小时，4-(3-(对甲苯磺酰)丙基)哌啶-1-羧酸叔丁酯(4.9g,12.34mmol)加入，反应液室温搅拌过夜。水(100mL)加入，用乙酸乙酯(100mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品经柱层析(PE:EA＝5:1)纯化得到4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙氧基)哌啶-1-羧酸苄酯。Benzyl 4-hydroxypiperidine-1-carboxylate (4.4 g, 18.51 mmol) was dissolved in dry DMF (10 mL) and cooled to 0 °C, NaH (0.6 g, 24.68 mmol) was added, stirred for 0.5 h, then room temperature After stirring for 1 hour, tert-butyl 4-(3-(p-toluenesulfonyl)propyl)piperidine-1-carboxylate (4.9 g, 12.34 mmol) was added, and the reaction solution was stirred at room temperature overnight. Water (100 mL) was added, extracted with ethyl acetate (100 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=5:1) to obtain 4-( Benzyl 3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propoxy)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝461.2. LC-MS: (ESI, m/z): [M+H] + = 461.2.
步骤3：4-(3-(哌啶-4-氧基)丙基)哌啶-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(3-(piperidin-4-oxy)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000935
Figure PCTCN2022088560-appb-000935
将4-(3-(1-(叔丁氧羰基)哌啶-4-基)丙氧基)哌啶-1-羧酸苄酯(540mg,1.17mmol)用乙酸乙酯(10mL)溶解，加入Pd(OH) 2/C(20％,170mg)，反应液加热到70℃搅拌3小时，冷却，过滤，固体用乙酸乙酯(20mL×3)洗三次，减压浓缩得到粗品4-(3-(哌啶-4-氧基)丙基)哌啶-1-羧酸叔丁酯。 Benzyl 4-(3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propoxy)piperidine-1-carboxylate (540 mg, 1.17 mmol) was dissolved in ethyl acetate (10 mL), Pd(OH) 2 /C (20%, 170 mg) was added, the reaction solution was heated to 70°C and stirred for 3 hours, cooled, filtered, the solid was washed three times with ethyl acetate (20 mL×3), and concentrated under reduced pressure to obtain the crude product 4-( 3-(Piperidin-4-oxy)propyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝327.3. LC-MS: (ESI, m/z): [M+H] + = 327.3.
步骤4：4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧基)丙基)哌啶-1-羧酸叔丁酯的制备Step 4: 4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy Preparation of tert-butyl)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000936
Figure PCTCN2022088560-appb-000936
将4-(3-(哌啶-4-氧基)丙基)哌啶-1-羧酸叔丁酯(150mg,0.46mmol)用DMSO(10mL)溶解，分别加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(200mg,0.46mmol)和DIEA(178mg,1.38mmol)，反应液室温搅拌2小时，加入水(50mL)，用乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品经柱层析(PE:EA＝1:10)纯化得到4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧基)丙基)哌啶-1-羧酸叔丁酯。4-(3-(Piperidin-4-oxy)propyl)piperidine-1-carboxylate tert-butyl ester (150 mg, 0.46 mmol) was dissolved in DMSO (10 mL), and 4-chloro-3-( 2,4-Dioxotetrahydropyrimidin-1(2H)-yl)pentafluorophenyl benzoate (200 mg, 0.46 mmol) and DIEA (178 mg, 1.38 mmol), the reaction solution was stirred at room temperature for 2 hours, and water (50 mL) was added. ), extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:10) to obtain 4-(3-(( 1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy)propyl)piperidine-1- tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝577.3. LC-MS: (ESI, m/z): [M+H] + = 577.3.
步骤5：1-(2-氯-5-(4-(3-(哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(2-Chloro-5-(4-(3-(piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H, Preparation of 3H)-dione
Figure PCTCN2022088560-appb-000937
Figure PCTCN2022088560-appb-000937
将4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧基)丙基)哌啶-1-羧酸叔丁酯(220mg,0.58mmol)用DCM(5mL)溶解，加入TFA(1mL)，反应液室温搅拌过夜，减压浓缩，用水(10mL)稀释，缓慢滴加饱和碳酸氢钠溶液，将反应液调至中性，用乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩得到粗品1-(2-氯-5-(4-(3-(哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy) Propyl)piperidine-1-carboxylate tert-butyl ester (220 mg, 0.58 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, the reaction solution was stirred at room temperature overnight, concentrated under reduced pressure, diluted with water (10 mL), slowly dropped Saturated sodium bicarbonate solution was added, the reaction solution was adjusted to neutrality, extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain crude 1-(2-chloro-5- (4-(3-(Piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝477.2. LC-MS: (ESI, m/z): [M+H] + = 477.2.
步骤6：1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(2-Chloro-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000938
Figure PCTCN2022088560-appb-000938
将1-(2-氯-5-(4-(3-(哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(71mg,0.14mmol)，HATU(63mg,0.17mmol)和DIEA(54mg,0.42mmol)加入到(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(80mg,0.14mmol)的DMF(10mL)溶液中，反应液室温搅拌2小时，加入水(100mL)，用乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品使用反相制备纯化得到1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(4-(3-(piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H) - Diketone (71 mg, 0.14 mmol), HATU (63 mg, 0.17 mmol) and DIEA (54 mg, 0.42 mmol) were added to (1R,4R)-4-(4-((((R)-1-(4-( 2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cycle In a solution of hexane-1-carboxylic acid (80 mg, 0.14 mmol) in DMF (10 mL), the reaction solution was stirred at room temperature for 2 hours, water (100 mL) was added, extracted with ethyl acetate (25 mL×4), washed with saturated brine, no It was dried over sodium sulfate, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(2-chloro-5-(4-(3-(1-((1R,4R)-4-(4-((((R )-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinoline oxazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dihydropyrimidine ketone.
LC-MS:(ESI,m/z):[M+H] +＝1051.4. LC-MS: (ESI, m/z): [M+H] + = 1051.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.31(d,J＝8.4Hz,1H),8.06(s,1H),7.64(d,J＝8.2Hz,1H),7.57(s,1H),7.42(d,J＝8.5Hz,2H),7.36(d,J＝7.8Hz,1H),7.24(s,1H),7.02(s,1H),6.97(s,1H),5.97(s,1H),4.45-4.35(m,1H),3.98-3.84(m,5H),3.82-3.71(m,1H),3.67-3.57(m,1H),3.61-3.50(m,2H),3.41(t,J＝6.3Hz,3H),3.18-2.90(m,6H),2.78-2.70(m,1H),2.70-2.60(m,1H),2.43(s,3H),2.02(s,6H),1.90-1.40(m,20H),1.30-1.21(m,2H),1.08-0.87(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ 10.50(s, 1H), 8.31(d, J=8.4Hz, 1H), 8.06(s, 1H), 7.64(d, J=8.2Hz, 1H) ,7.57(s,1H),7.42(d,J=8.5Hz,2H),7.36(d,J=7.8Hz,1H),7.24(s,1H),7.02(s,1H),6.97(s, 1H), 5.97(s, 1H), 4.45-4.35(m, 1H), 3.98-3.84(m, 5H), 3.82-3.71(m, 1H), 3.67-3.57(m, 1H), 3.61-3.50( m, 2H), 3.41(t, J＝6.3Hz, 3H), 3.18-2.90(m, 6H), 2.78-2.70(m, 1H), 2.70-2.60(m, 1H), 2.43(s, 3H) ,2.02(s,6H),1.90-1.40(m,20H),1.30-1.21(m,2H),1.08-0.87(m,2H).
实施例55：1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 55: 1-(2-Chloro-5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(1,1-dioxide) (2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl )piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000939
Figure PCTCN2022088560-appb-000939
4-(4-((1-(1,1-二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(70mg,0.14mmol)用DMF(3mL)溶解，1-(2-氯-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(73.3mg,0.15mmol)，HATU(79.8mg,0.21mmol)和DIEA(91mg,0.7mmol)分别加入，反应液室温搅拌1小时，用水(40mL)稀释，乙酸乙酯(40mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(4-((1-(1,1-Dioxide-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methyl quinazolin-6-yl)cyclohexane-1-carboxylic acid (70 mg, 0.14 mmol) was dissolved in DMF (3 mL), 1-(2-chloro-5-(4-((2-(piperidine- 4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (73.3 mg, 0.15 mmol), HATU (79.8 mg, 0.21 mmol) and DIEA (91 mg, 0.7 mmol) were added respectively, the reaction solution was stirred at room temperature for 1 hour, diluted with water (40 mL), extracted with ethyl acetate (40 mL×3), the organic phase was washed with saturated brine (40 mL), and anhydrous sulfuric acid It was dried over sodium, concentrated under reduced pressure, and the crude product was purified by prep-HPLC to give 1-(2-chloro-5-(4-((2-(1-((1R,4R)-4-(4-((((R)) -1-(1,1-Dioxide-2,3-dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6 -yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione .
LC-MS:(ESI,m/z):[M+H] +＝968.4. LC-MS: (ESI, m/z): [M+H] + = 968.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.27(d,J＝7.0Hz,1H),8.06(s,1H),7.80(d,J＝7.6Hz,1H),7.67-7.57(m,2H),7.56–7.48(m,2H),7.38(d,J＝8.4Hz,1H),6.98(s,1H),5.59(t,J＝7.4Hz,1H),4.39(d,J＝11.8Hz,2H),3.91(s,1H),3.87(s,3H),3.81-3.70(m,2H),3.67–3.59(m,3H),3.54-3.46(m,1H),3.42(t,J＝6.4Hz,2H),3.29(s,1H),3.24(d,J＝6.4Hz,2H),3.11–2.90(m,3H),2.82-2.62(m,4H),2.32(s,3H),2.12–1.23(m,20H),1.20-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.27(d, J=7.0Hz, 1H), 8.06(s, 1H), 7.80(d, J=7.6Hz, 1H) ,7.67-7.57(m,2H),7.56-7.48(m,2H),7.38(d,J=8.4Hz,1H),6.98(s,1H),5.59(t,J=7.4Hz,1H), 4.39(d, J＝11.8Hz, 2H), 3.91(s, 1H), 3.87(s, 3H), 3.81-3.70(m, 2H), 3.67-3.59(m, 3H), 3.54-3.46(m, 1H), 3.42(t, J=6.4Hz, 2H), 3.29(s, 1H), 3.24(d, J=6.4Hz, 2H), 3.11-2.90(m, 3H), 2.82-2.62(m, 4H) ), 2.32(s, 3H), 2.12-1.23(m, 20H), 1.20-0.90(m, 4H).
实施例56：1-(2-氯-5-(4-(4-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 56: 1-(2-Chloro-5-(4-(4-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(4-(4-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(4-(4-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperazin-1-yl)butyl ) Preparation of piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000940
Figure PCTCN2022088560-appb-000940
将4-(4-(哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(100mg,0.31mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(133mg,0.31mmol)溶于DMSO(3mL)中，搅拌下加入DIEA(198mg,1.54mmol)，室温下搅拌1小时。反应结束后反应液倒入水(30mL)中，EA萃取(30mL×3)，合并有机相，并用饱和食盐水洗，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(DCM:MeOH＝10:1)纯化得到4-(4-(4-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯。4-(4-(Piperazin-1-yl)butyl)piperidine-1-carboxylate tert-butyl ester (100 mg, 0.31 mmol) and 4-chloro-3-(2,4-dioxotetrahydro Pyrimidine-1(2H)-yl)benzoic acid pentafluorophenyl ester (133 mg, 0.31 mmol) was dissolved in DMSO (3 mL), DIEA (198 mg, 1.54 mmol) was added with stirring, and the mixture was stirred at room temperature for 1 hour. After the reaction, the reaction solution was poured into water (30 mL), extracted with EA (30 mL×3), the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was subjected to column chromatography (DCM:MeOH= 10:1) Purification to give 4-(4-(4-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperazin-1-yl )butyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝576.3. LC-MS: (ESI, m/z): [M+H] + = 576.3.
步骤2：1-(2-氯-5-(4-(4-(哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Chloro-5-(4-(4-(piperidin-4-yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H )-dione preparation
Figure PCTCN2022088560-appb-000941
Figure PCTCN2022088560-appb-000941
将4-(4-(4-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(112mg,0.19mmol)溶于DCM(2mL)中,加入0.2mL TFA,反应液室温下反应1小时，直接减压浓缩得到1-(2-氯-5-(4-(4-(哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(4-(4-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperazin-1-yl)butyl)piperidine Pyridin-1-carboxylate tert-butyl ester (112 mg, 0.19 mmol) was dissolved in DCM (2 mL), 0.2 mL of TFA was added, the reaction solution was reacted at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain 1-(2-chloro-5- (4-(4-(Piperidin-4-yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝476.3 LC-MS: (ESI, m/z): [M+H] + = 476.3
步骤3：1-(2-氯-5-(4-(4-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-(4-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperidin-4-yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000942
Figure PCTCN2022088560-appb-000942
将1-(2-氯-5-(4-(4-(哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(165mg,0.195mmol)和(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(115mg,0.195mmol)，溶于DMF(3mL)中，搅拌下加入HATU(86mg,0.227mmol)和DIEA(75mg,0.584mmol)，室温下反应1h。反应结束后反应液倒入水(50mL)中，EA萃取(30mL×3)，合并有机相并用饱和食盐水洗涤，无水硫酸钠干燥，过滤，浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-(4-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丁基)哌嗪-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮.1-(2-Chloro-5-(4-(4-(piperidin-4-yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)- Diketone (165 mg, 0.195 mmol) and (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl) )thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (115 mg, 0.195 mmol) in DMF ( 3 mL), HATU (86 mg, 0.227 mmol) and DIEA (75 mg, 0.584 mmol) were added under stirring, and the reaction was carried out at room temperature for 1 h. After the reaction, the reaction solution was poured into water (50 mL), extracted with EA (30 mL×3), the organic phases were combined and washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by prep-HPLC to obtain 1-( 2-Chloro-5-(4-(4-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-Chloro-6-((dimethyl Amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine-4 -yl)butyl)piperazine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1050.7. LC-MS: (ESI, m/z): [M+H] + = 1050.7.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.30(d,J＝8.3Hz,1H),8.05(s,1H),7.64(d,J＝8.2Hz,1H),7.56(d,J＝2.0Hz,1H),7.46–7.30(m,4H),7.24(d,J＝1.4Hz,1H),7.02(s,1H),6.96(s,1H),5.96(dd,J＝14.4,7.2Hz,1H),4.40(d,J＝11.5Hz,1H),3.89(s,4H),3.78–3.71(m,1H),3.62(d,J＝6.0Hz,3H),3.11(d,J＝15.8Hz,2H),3.01-2.92(m,2H),2.76-2.63(m,2H),2.68–2.58(m,2H),2.42(s,6H),2.34–2.18(m,4H),2.01(s,6H),1.85(d,J＝9.6Hz,2H),1.79(d,J＝11.5Hz,2H),1.72(d,J＝7.0Hz,4H),1.65(d,J＝12.4Hz,2H),1.60–1.50(m,3H),1.42(d,J＝7.4Hz,3H),1.34–1.14(m,5H),1.02–0.82(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.30(d, J=8.3Hz, 1H), 8.05(s, 1H), 7.64(d, J=8.2Hz, 1H) ,7.56(d,J＝2.0Hz,1H),7.46–7.30(m,4H),7.24(d,J＝1.4Hz,1H),7.02(s,1H),6.96(s,1H),5.96( dd, J=14.4, 7.2Hz, 1H), 4.40 (d, J=11.5Hz, 1H), 3.89 (s, 4H), 3.78–3.71 (m, 1H), 3.62 (d, J=6.0Hz, 3H) ), 3.11(d, J＝15.8Hz, 2H), 3.01-2.92(m, 2H), 2.76-2.63(m, 2H), 2.68-2.58(m, 2H), 2.42(s, 6H), 2.34- 2.18(m, 4H), 2.01(s, 6H), 1.85(d, J=9.6Hz, 2H), 1.79(d, J=11.5Hz, 2H), 1.72(d, J=7.0Hz, 4H), 1.65(d,J=12.4Hz,2H),1.60-1.50(m,3H),1.42(d,J=7.4Hz,3H),1.34-1.14(m,5H),1.02-0.82(m,2H) .
实施例57：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 57: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-( (dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl) Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethyl)benzoyl)piperidine- Preparation of 4-yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000943
Figure PCTCN2022088560-appb-000943
将4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(100mg,0.31mmol)，3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲基)苯甲酸五氟苯酯(133mg,0.31mmol)溶于DMSO(3mL)中，搅拌下加入DIEA(198mg,1.54mmol)，室温下反应1小时。反应结束后用水(30mL)稀释，乙酸乙酯萃取(30mL×3)，合并有机相，饱和食盐水洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析分离得到4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。4-(2-(Piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (100 mg, 0.31 mmol), 3-(2,4-dioxotetrahydropyrimidine -1(2H)-yl)-4-(trifluoromethyl)benzoic acid pentafluorophenyl ester (133 mg, 0.31 mmol) was dissolved in DMSO (3 mL), DIEA (198 mg, 1.54 mmol) was added with stirring, and the mixture was stirred at room temperature. React for 1 hour. After the reaction, it was diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was separated by column chromatography to obtain 4-( 2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethyl)benzoyl)piperidin-4-yl)methoxy yl)ethyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+Na] +＝633.2. LC-MS: (ESI, m/z): [M+Na] + = 633.2.
步骤2：1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)di Preparation of Hydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000944
Figure PCTCN2022088560-appb-000944
将4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯(112mg，0.19mmol)溶于二氯甲烷(2mL)中，加入三氟乙酸(0.8mL)，反应液室温下反应1h。反应结束后反应液减压浓缩得到1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，无需纯化直接用于下一步反应。4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethyl)benzoyl)piperidine-4- tert-butyl) methoxy)ethyl)piperidine-1-carboxylate (112mg, 0.19mmol) was dissolved in dichloromethane (2mL), trifluoroacetic acid (0.8mL) was added, and the reaction solution was reacted at room temperature for 1h . After the reaction, the reaction solution was concentrated under reduced pressure to obtain 1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl) yl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione, which was used in the next reaction without purification.
步骤3：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-(() Dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine Preparation of pyridin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000945
Figure PCTCN2022088560-appb-000945
将1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(TFA盐，165mg,0.195mmol)和(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨 基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(115.3mg,0.195mmol)溶于DMF(3mL)中，搅拌下加入HATU(86.3mg,0.227mmol)和DIEA(75.4mg,0.584mmol)。反应液室温下反应1h。反应结束后用水(30mL)稀释，乙酸乙酯萃取(30mL×3)，合并有机相并用饱和食盐水洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用prep-HPLC纯化得到1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine -2,4(1H,3H)-dione (TFA salt, 165 mg, 0.195 mmol) and (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- The carboxylic acid (115.3 mg, 0.195 mmol) was dissolved in DMF (3 mL) and HATU (86.3 mg, 0.227 mmol) and DIEA (75.4 mg, 0.584 mmol) were added with stirring. The reaction solution was reacted at room temperature for 1 h. After the reaction was completed, it was diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), the organic phases were combined and washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by prep-HPLC to obtain 1-( 5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) (yl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl) Ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1085.5. LC-MS: (ESI, m/z): [M+H] + = 1085.5.
1H NMR(400MHz,DMSO-d 6)δ10.53(s,1H),8.31(d,J＝8.1Hz,1H),8.05(s,1H),7.87(d,J＝8.1Hz,1H),7.70(s,1H),7.58(d,J＝8.0Hz,1H),7.43(t,J＝8.0Hz,2H),7.37–7.31(m,1H),7.24(d,J＝1.3Hz,1H),7.02(s,1H),6.96(s,1H),6.00-5.92(m,1H),4.53-4.31(m,2H),3.94–3.82(m,5H),3.52-3.37(m,4H),3.23(d,J＝6.1Hz,2H),3.12(d,J＝2.1Hz,2H),3.07–2.90(m,3H),2.85-2.74(m,1H),2.72-2.58(m,3H),2.42(s,3H),2.01(s,6H),1.89-1.50(m,18H),1.48-1.40(m,2H),1.21-0.91(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.53 (s, 1H), 8.31 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.87 (d, J=8.1 Hz, 1H) ,7.70(s,1H),7.58(d,J＝8.0Hz,1H),7.43(t,J＝8.0Hz,2H),7.37–7.31(m,1H),7.24(d,J＝1.3Hz, 1H), 7.02(s, 1H), 6.96(s, 1H), 6.00-5.92(m, 1H), 4.53-4.31(m, 2H), 3.94-3.82(m, 5H), 3.52-3.37(m, 4H), 3.23(d, J=6.1Hz, 2H), 3.12(d, J=2.1Hz, 2H), 3.07-2.90(m, 3H), 2.85-2.74(m, 1H), 2.72-2.58(m ,3H),2.42(s,3H),2.01(s,6H),1.89-1.50(m,18H),1.48-1.40(m,2H),1.21-0.91(m,4H).
实施例58：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 58: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-( (dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl) Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲氧基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethoxy)benzoyl)piperidine Preparation of -4-yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000946
Figure PCTCN2022088560-appb-000946
将3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲氧基)苯甲酸五氟苯酯(150mg,0.31mmol)和4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(100mg,0.31mmol)溶于DMSO(3mL)中，搅拌下加入DIEA(198mg,1.54mmol)，室温下搅拌1小时。反应结束后反应液倒入水(30mL)中，EA萃取(30mL×3)，合并有机相，并用饱和食盐水洗，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(DCM:MeOH＝10:1)纯化得到4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲氧基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。3-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethoxy)benzoic acid pentafluorophenyl ester (150 mg, 0.31 mmol) and 4-(2- (Piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (100 mg, 0.31 mmol) was dissolved in DMSO (3 mL), DIEA (198 mg, 1.54 mmol) was added with stirring, room temperature under stirring for 1 hour. After the reaction, the reaction solution was poured into water (30 mL), extracted with EA (30 mL×3), the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was subjected to column chromatography (DCM:MeOH= 10:1) Purification to give 4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethoxy)benzoyl) ) piperidin-4-yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+Na] +＝649.3. LC-MS: (ESI, m/z): [M+Na] + = 649.3.
步骤2：1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(5-(4-((2-(Piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl) Preparation of dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000947
Figure PCTCN2022088560-appb-000947
将4-(2-((1-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-(三氟甲氧基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯(110mg,0.17mmol)溶于DCM(2mL)中，加入TFA(0.2mL)，反应液室温下反应1小时，直接减压浓缩得到1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(2-((1-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-(trifluoromethoxy)benzoyl)piperidine-4 -yl)methoxy)ethyl)piperidine-1-carboxylate tert-butyl ester (110 mg, 0.17 mmol) was dissolved in DCM (2 mL), TFA (0.2 mL) was added, the reaction solution was reacted at room temperature for 1 hour, and the Concentration under reduced pressure gave 1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl ) dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝527.3 LC-MS: (ESI, m/z): [M+H] + = 527.3
步骤3：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-(() Dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine Preparation of pyridin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000948
Figure PCTCN2022088560-appb-000948
将1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(90mg,0.17mmol)和(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(100mg,0.17mmol)，溶于DMF(3mL)中，搅拌下加入HATU(84mg,0.22mmol)和DIEA(66mg,0.51mmol)，室温下反应1h。反应结束后反应液倒入水(50mL)中，EA萃取(30mL×3)，合并有机相并用饱和食盐水洗涤，无水硫酸钠干燥，过滤，浓缩，粗品使用prep-HPLC纯化得到1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲氧基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl)dihydro Pyrimidine-2,4(1H,3H)-dione (90 mg, 0.17 mmol) and (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-( (Dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (100 mg, 0.17 mmol), dissolved in DMF (3 mL), added HATU (84 mg, 0.22 mmol) and DIEA (66 mg, 0.51 mmol) under stirring, and reacted at room temperature for 1 h. After the reaction, the reaction solution was poured into water (50 mL), extracted with EA (30 mL×3), the organic phases were combined and washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by prep-HPLC to obtain 1-( 5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) (yl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl) Ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethoxy)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1101.5. LC-MS: (ESI, m/z): [M+H] + = 1101.5.
1H NMR(400MHz,DMSO-d 6)δ10.54(s,1H),8.31(d,J＝8.2Hz,1H),8.05(s,1H),7.59(d,J＝2.0Hz,1H),7.52(dd,J＝8.4,1.4Hz,1H),7.49-7.30(m,4H),7.24(d,J＝1.3Hz,1H),7.02(s,1H),6.96(s,1H),6.02–5.91(m,1H),4.52–4.33(m,2H),3.98-3.90(m,4H),3.80-3.65(m,2H),3.61-3.51(m,1H),3.41(t,J＝6.3Hz,2H),3.23(d,J＝6.2Hz,2H),3.15–2.89(m,5H),2.82-2.60(m,4H),2.42(s,3H),2.01(s,6H),1.89–1.40(m,20H),1.20-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ 10.54(s, 1H), 8.31(d, J=8.2Hz, 1H), 8.05(s, 1H), 7.59(d, J=2.0Hz, 1H) ,7.52(dd,J＝8.4,1.4Hz,1H),7.49-7.30(m,4H),7.24(d,J＝1.3Hz,1H),7.02(s,1H),6.96(s,1H), 6.02-5.91(m,1H), 4.52-4.33(m,2H), 3.98-3.90(m,4H), 3.80-3.65(m,2H), 3.61-3.51(m,1H), 3.41(t,J =6.3Hz,2H),3.23(d,J=6.2Hz,2H),3.15-2.89(m,5H),2.82-2.60(m,4H),2.42(s,3H),2.01(s,6H) ,1.89-1.40(m,20H),1.20-0.90(m,4H).
实施例59：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 59: 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) (ylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-((4-((苄氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 9-((4-((benzyloxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000949
Figure PCTCN2022088560-appb-000949
9-醛基-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(300mg,1.06mmol)和哌嗪-1-羧酸苄酯(235mg,1.06mmol)用四氢呋喃(10mL)溶解，搅拌下加入三乙酰氧基硼氢化钠(674mg,3.18mmol)。室温下搅拌2小时后，加水(50mL)，用二氯甲烷(30mLx3)提取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到9-((4-((苄氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。9-Aldol-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (300 mg, 1.06 mmol) and benzyl piperazine-1-carboxylate (235 mg, 1.06 mmol) were treated with tetrahydrofuran (10 mL) ) was dissolved, and sodium triacetoxyborohydride (674 mg, 3.18 mmol) was added with stirring. After stirring at room temperature for 2 hours, water (50 mL) was added, extracted with dichloromethane (30 mL×3), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography ( Methanol:dichloromethane=1:9) purification to give 9-((4-((benzyloxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 - tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝486.2. LC-MS: (ESI, m/z): [M+H] + = 486.2.
步骤2：9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-000950
Figure PCTCN2022088560-appb-000950
9-((4-((苄氧基)羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(500mg,1.02mmol)溶解于乙酸乙酯(15mL)中，加入Pd(OH) 2/C(250mg,0.35mmol)，在氢气氛围下升温至70℃，搅拌过夜。反应液冷却至室温，过滤，滤液减压浓缩得到9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯，粗品无需纯化直接用于下一步反应。 9-((4-((benzyloxy)carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (500 mg, 1.02 mmol) It was dissolved in ethyl acetate (15 mL), Pd(OH) 2 /C (250 mg, 0.35 mmol) was added, the temperature was raised to 70° C. under a hydrogen atmosphere, and the mixture was stirred overnight. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain 9-(piperazin-1-ylmethyl)-3-azaspiro[5.5]undecane-3-carboxylic acid tert-butyl ester. The crude product was directly used for the next reaction.
LC-MS:(ESI,m/z):[M+H] +＝352.2. LC-MS: (ESI, m/z): [M+H] + = 352.2.
步骤3：9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 3: 9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)benzene (yl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl) Preparation of -3-azaspiro[5.5]undecane-3-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000951
Figure PCTCN2022088560-appb-000951
9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(130mg,0.36mmol)溶解于DMF(10mL)中，加入(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(200mg,0.33mmol)，HATU(188mg,0.49mmol)和DIEA(127mg,0.99mmol)，室温下搅拌1小时。反应液加入水(100mL)，用乙酸乙酯(3x 30mL)提取，有机相用饱和食盐水(100mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。9-(Piperazin-1-ylmethyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester (130 mg, 0.36 mmol) was dissolved in DMF (10 mL), (1R, 4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (200 mg, 0.33 mmol), HATU (188 mg, 0.49 mmol) and DIEA (127 mg, 0.99 mmol), Stir at room temperature for 1 hour. The reaction solution was added with water (100 mL), extracted with ethyl acetate (3×30 mL), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (methanol: Dichloromethane=1:9) purification to give 9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) (ylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝926.4. LC-MS: (ESI, m/z): [M+H] + = 926.4.
步骤4：(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮的制备Step 4: (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R )-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinoline Preparation of oxazolin-6-yl)cyclohexyl)methanone
Figure PCTCN2022088560-appb-000952
Figure PCTCN2022088560-appb-000952
9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(230mg,0.25mmol)溶解于DCM(3mL)中，加入TFA(1mL)，室温下搅拌2小时。反应液直接减压浓缩得到(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮。9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophene -2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3- Azaspiro[5.5]undecane-3-carboxylate tert-butyl ester (230 mg, 0.25 mmol) was dissolved in DCM (3 mL), TFA (1 mL) was added, and the mixture was stirred at room temperature for 2 hours. The reaction solution was directly concentrated under reduced pressure to obtain (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4- (((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝826.5. LC-MS: (ESI, m/z): [M+H] + = 826.5.
步骤5：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) Amino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1 Preparation of -yl)methyl)-3-azaspiro[5.5]undecane-3-carbonyl)-2-methoxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000953
Figure PCTCN2022088560-appb-000953
(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基) 噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(110mg,0.12mmol)溶于DMSO(10mL)中，加入3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯(57mg,0.13mmol)和DIEA(46mg,0.36mmol)，室温下搅拌2小时。向反应液加入水(100mL)，用二氯甲烷(30mLx3)萃取，有机相用饱和氯化钠水溶液(100mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩得到粗品。粗品经pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-甲氧基苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)-1 -(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexyl)methanone (110 mg, 0.12 mmol) was dissolved in DMSO (10 mL), 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxy was added Pentafluorophenyl benzoate (57 mg, 0.13 mmol) and DIEA (46 mg, 0.36 mmol) were stirred at room temperature for 2 hours. Water (100 mL) was added to the reaction solution, extracted with dichloromethane (30 mL×3), the organic phase was washed with saturated aqueous sodium chloride solution (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain the crude product. The crude product was purified by pre-HPLC ( CH3CN /0.08% aqueous NH4HCO3 , 5 %~95%) to give 1-(5-(9-((4-((1R,4R)-4-(4- (((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-methyl oxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1072.5. LC-MS: (ESI, m/z): [M+H] + = 1072.5.
1H NMR(400MHz,DMSO-d 6)δ10.32(s,1H),8.32(d,J＝8.1Hz,1H),8.05(s,1H),7.43(t,J＝8.1Hz,2H),7.38–7.33(m,2H),7.32(d,J＝2.0Hz,1H),7.24(s,1H),7.15(d,J＝8.6Hz,1H),7.02(s,1H),6.96(s,1H),6.00–5.92(m,1H),3.89(s,3H),3.84(s,3H),3.59(t,J＝6.6Hz,2H),3.49-3.37(m,4H),3.17–3.09(m,2H),2.94(t,J＝12.0Hz,1H),2.68(t,J＝6.6Hz,2H),2.65-2.43(m,2H),2.42(s,3H),2.33-2.26(m,4H),2.16-2.08(m,2H),2.02(s,6H),1.83-1.46(m,21H),1.35-1.24(m,2H),1.16-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.32(s, 1H), 8.32(d, J=8.1Hz, 1H), 8.05(s, 1H), 7.43(t, J=8.1Hz, 2H) ,7.38–7.33(m,2H),7.32(d,J＝2.0Hz,1H),7.24(s,1H),7.15(d,J＝8.6Hz,1H),7.02(s,1H),6.96( s,1H),6.00-5.92(m,1H),3.89(s,3H),3.84(s,3H),3.59(t,J＝6.6Hz,2H),3.49-3.37(m,4H),3.17 –3.09(m, 2H), 2.94(t, J=12.0Hz, 1H), 2.68(t, J=6.6Hz, 2H), 2.65-2.43(m, 2H), 2.42(s, 3H), 2.33- 2.26(m, 4H), 2.16-2.08(m, 2H), 2.02(s, 6H), 1.83-1.46(m, 21H), 1.35-1.24(m, 2H), 1.16-0.90(m, 4H).
实施例60：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 60: 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethyl) (ylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-fluorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000954
Figure PCTCN2022088560-appb-000954
(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)甲酮(110mg,0.12mmol)溶于DMSO(5mL)中，加3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酸五氟苯酯(54mg,0.13mmol)和DIEA(46mg,0.36mmol)，室温下搅拌2小时。向反应液加入水(50mL)，用二氯甲烷(30mLx3)提取，有机相用饱和氯化钠水溶液(50mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩得到粗品。粗品经pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氟苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)-1 -(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline- 6-yl)cyclohexyl)methanone (110 mg, 0.12 mmol) was dissolved in DMSO (5 mL), 3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzene was added Pentafluorophenyl formate (54 mg, 0.13 mmol) and DIEA (46 mg, 0.36 mmol) were stirred at room temperature for 2 hours. Water (50 mL) was added to the reaction solution, extracted with dichloromethane (30 mL×3), the organic phase was washed with saturated aqueous sodium chloride solution (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain the crude product. The crude product was purified by pre-HPLC ( CH3CN /0.08% aqueous NH4HCO3 , 5 %~95%) to give 1-(5-(9-((4-((1R,4R)-4-(4- (((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-fluoro Phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1060.5. LC-MS: (ESI, m/z): [M+H] + = 1060.5.
1H NMR(400MHz,DMSO-d 6)δ10.52(s,1H),8.32(d,J＝8.3Hz,1H),8.05(s,1H),7.50(d,J＝7.9Hz,1H),7.38(m,5H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.04–5.88(m,1H),3.89(s,3H),3.75(t,J＝6.6Hz,2H),3.57(s,2H),3.46(s,4H),3.30–3.26(m,1H),3.11(d,J＝15.1Hz,2H),2.94(m,1H),2.73(t,J＝6.6Hz,2H),2.63(m,1H),2.42(s,3H),2.32(s,2H),2.29(s,2H),2.11(s,2H),2.01(s,6H),1.90–1.39(m,19H),1.34(m,2H),1.07(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.52(s, 1H), 8.32(d, J=8.3Hz, 1H), 8.05(s, 1H), 7.50(d, J=7.9Hz, 1H) ,7.38(m,5H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.04–5.88(m,1H),3.89(s,3H),3.75(t,J ＝6.6Hz, 2H), 3.57(s, 2H), 3.46(s, 4H), 3.30–3.26(m, 1H), 3.11(d, J＝15.1Hz, 2H), 2.94(m, 1H), 2.73 (t, J＝6.6Hz, 2H), 2.63(m, 1H), 2.42(s, 3H), 2.32(s, 2H), 2.29(s, 2H), 2.11(s, 2H), 2.01(s, 6H), 1.90–1.39(m, 19H), 1.34(m, 2H), 1.07(m, 4H).
实施例61：1-(2-氯-5-(4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 61: 1-(2-Chloro-5-(4-(3-((1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro) -6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperidin-4-yl)oxy)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(3-((1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethylamino)meth) ) (yl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl) Preparation of tert-butyl oxy)propyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000955
Figure PCTCN2022088560-appb-000955
将4-(3-(哌啶-4-氧基)丙基)哌啶-1-羧酸叔丁酯(105mg,0.32mmol)，HATU(145mg,0.38mmol)和DIEA(123mg,0.96mmol)加入到(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(190mg,0.32mmol)的DMF(5mL)溶液中，室温搅拌2小时，用水(50mL)稀释，乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，得到粗品4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羧酸叔丁酯。4-(3-(Piperidin-4-oxy)propyl)piperidine-1-carboxylate tert-butyl ester (105 mg, 0.32 mmol), HATU (145 mg, 0.38 mmol) and DIEA (123 mg, 0.96 mmol) Added to (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl) A solution of ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (190 mg, 0.32 mmol) in DMF (5 mL) was stirred at room temperature for 2 hours , diluted with water (50 mL), extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give crude product 4-(3-((1-((1R,4R)-4 -(4-(((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methyl Oxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)oxy)propyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝901.4. LC-MS: (ESI, m/z): [M+H] + = 901.4.
步骤2：((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙氧基)哌啶-1-基)甲酮的制备Step 2: ((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophene-2- yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propoxy)piperidine- Preparation of 1-yl)methanone
Figure PCTCN2022088560-appb-000956
Figure PCTCN2022088560-appb-000956
将4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羧酸叔丁酯(170mg,0.19mmol)用DCM(5mL)溶解，加入TFA(1mL)，室温搅拌2小时，反应液直接减压浓缩得到粗品((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙氧基)哌啶-1-基)甲酮。4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) Phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)oxy) Propyl)piperidine-1-carboxylate tert-butyl ester (170 mg, 0.19 mmol) was dissolved in DCM (5 mL), TFA (1 mL) was added, stirred at room temperature for 2 hours, the reaction solution was directly concentrated under reduced pressure to obtain the crude product ((1R, 4R )-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propoxy)piperidin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝801.4. LC-MS: (ESI, m/z): [M+H] + = 801.4.
步骤3：1-(2-氯-5-(4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 Preparation of -carbonyl)piperidin-4-yl)oxy)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000957
Figure PCTCN2022088560-appb-000957
将((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(3-(哌啶-4-基)丙氧基)哌啶-1-基)甲酮(150mg,0.19mmol)用DMSO(10mL)溶解，分别加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(97mg,0.23mmol)和DIEA(72mg,0.56mmol)，室温搅拌2小时，用水(50mL)稀释，乙酸乙酯(25mL×4)萃取，饱和食盐水洗净，无水硫酸钠干燥，减压浓缩，粗品使用反相制备纯化得到1-(2-氯-5-(4-(3-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)氧)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl) Ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(3-(piperidin-4-yl)propoxy)piperidine-1- yl)methanone (150 mg, 0.19 mmol) was dissolved in DMSO (10 mL), and 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl was added separately (97 mg, 0.23 mmol) and DIEA (72 mg, 0.56 mmol), stirred at room temperature for 2 hours, diluted with water (50 mL), extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, and reduced pressure. Concentrated and the crude product was purified using reverse phase preparation to give 1-(2-chloro-5-(4-(3-((1-((1R,4R)-4-(4-((((R)-1-(4) -(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl ) cyclohexane-1-carbonyl)piperidin-4-yl)oxy)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1051.4. LC-MS: (ESI, m/z): [M+H] + = 1051.4.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.30(d,J＝8.2Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.7Hz,1H),7.48–7.30(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.03-5.87(m,1H),4.53-4.33(m,1H),3.93-3.81(m,4H),3.79-3.45(m,5H),3.41(t,J＝6.2Hz,2H),3.27–3.20(m,1H),3.18–2.99(m,4H),2.99-2.89(m,1H),2.80-2.60(m,4H),2.42(s,3H),2.01(s,6H),1.88–1.23(m,22H),1.10-1.00(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.49(s, 1H), 8.30(d, J=8.2Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝1.7Hz,1H),7.48-7.30(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.03-5.87(m,1H) ), 4.53-4.33(m, 1H), 3.93-3.81(m, 4H), 3.79-3.45(m, 5H), 3.41(t, J=6.2Hz, 2H), 3.27-3.20(m, 1H), 3.18-2.99(m,4H), 2.99-2.89(m,1H), 2.80-2.60(m,4H), 2.42(s,3H), 2.01(s,6H), 1.88-1.23(m,22H), 1.10-1.00(m,2H).
实施例62：1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 62: 1-(2-Chloro-5-(9-(2-(4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)哌啶-1-羧酸(9H-芴-9-基)甲酯的制备Step 1: Preparation of 4-(2-(3-azaspiro[5.5]undecan-9-yl)ethyl)piperidine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester
Figure PCTCN2022088560-appb-000958
Figure PCTCN2022088560-appb-000958
将化合物9-(2-(4-(((9H-芴-9-基)甲氧基)羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(70mg,0.12mmol)溶于氯化氢的1,4-二氧六环(4M,7mL)溶液中，室温搅拌1小时，直接减压浓缩得到4-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)哌啶-1-羧酸(9H-芴-9-基)甲酯。Compound 9-(2-(4-(((9H-fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecane- 3-Carboxylic acid tert-butyl ester (70 mg, 0.12 mmol) was dissolved in a solution of hydrogen chloride in 1,4-dioxane (4M, 7 mL), stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain 4-(2-(3 - azaspiro[5.5]undecan-9-yl)ethyl)piperidine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝488.5. LC-MS: (ESI, m/z): [M+H] + = 488.5.
步骤2：4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羧酸(9H-芴-9-基)甲酯的制备Step 2: 4-(2-(3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5] Preparation of undecyl-9-yl)ethyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester
Figure PCTCN2022088560-appb-000959
Figure PCTCN2022088560-appb-000959
4-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)哌啶-1-羧酸(9H-芴-9-基)甲酯(70mg,0.12mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(52mg,0.12mmol)用DMSO(4mL)溶解，加入DIPEA(46mg,0.36mmol)，反应液室温搅拌过夜。用水(40mL)稀释，乙酸乙酯(30mL×2)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(EA in PE＝0-4:1)纯化得到4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羧酸(9H-芴-9-基)甲酯。4-(2-(3-Azaspiro[5.5]undecan-9-yl)ethyl)piperidine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester (70 mg, 0.12 mmol) and Pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (52 mg, 0.12 mmol) was dissolved in DMSO (4 mL) and DIPEA (46 mg, 0.36 mg) was added. mmol), the reaction solution was stirred at room temperature overnight. It was diluted with water (40 mL), extracted with ethyl acetate (30 mL×2), dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by column chromatography (EA in PE=0-4:1) to obtain 4-(2-( 3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)ethane yl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝738.5. LC-MS: (ESI, m/z): [M+H] + = 738.5.
步骤3：1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(9-(2-(piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)di Preparation of Hydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000960
Figure PCTCN2022088560-appb-000960
4-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)哌嗪-1-羧酸(9H-芴-9-基)甲酯(70mg,0.09mmol)用DCM(2mL)溶解，加入哌啶(0.3mL)，反应液室温搅拌3小时，用水(20mL)稀释，二氯甲烷(30mL×2)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(DCM:MeOH＝95:5)纯化得到1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(2-(3-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecane -9-yl)ethyl)piperazine-1-carboxylic acid (9H-fluoren-9-yl)methyl ester (70 mg, 0.09 mmol) was dissolved in DCM (2 mL), piperidine (0.3 mL) was added, and the reaction solution was room temperature Stirred for 3 hours, diluted with water (20 mL), extracted with dichloromethane (30 mL×2), dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by column chromatography (DCM:MeOH=95:5) to obtain 1-(2 -Chloro-5-(9-(2-(piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione.
LC-MS:(ESI,m/z):[M+Na] +＝516.3. LC-MS: (ESI, m/z): [M+Na] + = 516.3.
步骤4：1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧 啶-2,4(1H,3H)-二酮的制备Step 4: 1-(2-Chloro-5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000961
Figure PCTCN2022088560-appb-000961
1-(2-氯-5-(9-(2-(哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(30mg,0.06mmol)和(1R,4R)-4-(4-(((R)-1-(4-(2-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(34mg,0.06mmol)用DMF(3mL)溶解，加入HATU(27mg,0.07mmol)和DIEA(23mg,0.18mmol)，反应液室温搅拌过夜。用水(30mL)稀释，乙酸乙酯(30mL×3)萃取，无水硫酸钠干燥，减压，浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(9-(2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(9-(2-(piperazin-1-yl)ethyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine- 2,4(1H,3H)-dione (30 mg, 0.06 mmol) and (1R,4R)-4-(4-(((R)-1-(4-(2-((dimethylamino) Methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (34 mg, 0.06 mmol) It was dissolved in DMF (3 mL), HATU (27 mg, 0.07 mmol) and DIEA (23 mg, 0.18 mmol) were added, and the reaction solution was stirred at room temperature overnight. It was diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), dried over anhydrous sodium sulfate, reduced under reduced pressure, and concentrated. The crude product was purified by prep-HPLC to obtain 1-(2-chloro-5-(9-(2-( 4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl )ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethyl)-3-azaspiro[ 5.5] Undecane-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1090.5. LC-MS: (ESI, m/z): [M+H] + = 1090.5.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.30(d,J＝8.1Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(s,1H),7.47–7.28(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.00-5.92(m,1H),3.89(s,3H),3.80-3.71(m,1H),3.66-3.42(m,8H),3.12(s,2H),3.00-2.90(m,1H),2.78-2.71(m,2H),2.65-2.57(m,2H),2.42(s,3H),2.36-2.23(m,6H),2.01(s,6H),1.89-1.75(m,4H),1.72-1.29(m,18H),1.16-1.00(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50 (s, 1H), 8.30 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.63 (d, J=8.2 Hz, 1H) ,7.54(s,1H),7.47–7.28(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.00-5.92(m,1H),3.89(s ,3H),3.80-3.71(m,1H),3.66-3.42(m,8H),3.12(s,2H),3.00-2.90(m,1H),2.78-2.71(m,2H),2.65-2.57 (m,2H),2.42(s,3H),2.36-2.23(m,6H),2.01(s,6H),1.89-1.75(m,4H),1.72-1.29(m,18H),1.16-1.00 (m,4H).
实施例63：1-(5-(4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 63: 1-(5-(4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl) yl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl )amino)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-羟基丙基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(3-hydroxypropyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000962
Figure PCTCN2022088560-appb-000962
将3-(哌啶-4-基)丙烷-1-醇(700mg,4.9mmol)溶于1,4-二氧六环(7mL)中，然后加入Boc酸酐(2.1g,9.8mmol)和DMAP(30mg,0.24mmol)，反应液加热到80℃过夜。反应结束后倒入水(60mL)中，乙酸乙酯(30mL×3)萃取，无水硫酸钠干燥，有机相旋干，粗品使用柱层析(EA:PE＝0-3:7)纯化得到4-(3-羟基丙基)哌啶-1-羧酸叔丁酯。3-(Piperidin-4-yl)propan-1-ol (700 mg, 4.9 mmol) was dissolved in 1,4-dioxane (7 mL), then Boc anhydride (2.1 g, 9.8 mmol) and DMAP were added (30 mg, 0.24 mmol), and the reaction was heated to 80°C overnight. After the reaction, it was poured into water (60 mL), extracted with ethyl acetate (30 mL×3), dried over anhydrous sodium sulfate, the organic phase was spin-dried, and the crude product was purified by column chromatography (EA:PE=0-3:7) to obtain 4-(3-Hydroxypropyl)piperidine-1-carboxylate tert-butyl ester.
1H NMR(400MHz,DMSO-d 6)δ4.34(t,J＝5.1Hz,1H),3.91(d,J＝12.3Hz,2H),3.37(dd,J＝11.9,6.3Hz,2H),2.66(s,2H),1.61(d,J＝12.3Hz,2H),1.50–1.28(m,12H),1.20(dd,J＝15.2,6.9Hz,2H),0.93(m,2H). 1 H NMR (400 MHz, DMSO-d 6 ) δ 4.34 (t, J=5.1 Hz, 1H), 3.91 (d, J=12.3 Hz, 2H), 3.37 (dd, J=11.9, 6.3 Hz, 2H) ,2.66(s,2H),1.61(d,J=12.3Hz,2H),1.50–1.28(m,12H),1.20(dd,J=15.2,6.9Hz,2H),0.93(m,2H).
步骤2：4-(3-丙醛)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-(3-propanal)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000963
Figure PCTCN2022088560-appb-000963
把4-(3-羟基丙基)哌啶-1-羧酸叔丁酯(300mg,1.2mmol)溶于乙腈(5mL)，然后加入IBX(567mg,2.4mmol)，反应液加热到70℃反应2个小时，过滤，滤饼用乙酸乙酯(10mL×2)洗涤，有机相旋干，粗品使用柱层析(EA:PE＝0-1:4)纯化得到4-(3-丙醛)哌啶-1-羧酸叔丁酯。Dissolve 4-(3-hydroxypropyl)piperidine-1-carboxylate tert-butyl ester (300 mg, 1.2 mmol) in acetonitrile (5 mL), then add IBX (567 mg, 2.4 mmol), and heat the reaction solution to 70 °C to react 2 hours, filtered, the filter cake was washed with ethyl acetate (10 mL×2), the organic phase was spin-dried, and the crude product was purified by column chromatography (EA:PE=0-1:4) to obtain 4-(3-propanal) tert-Butyl piperidine-1-carboxylate.
1H NMR(400MHz,DMSO-d 6)δ9.68(t,J＝1.5Hz,1H),3.91(d,J＝12.0Hz,2H),2.65(m,2H),2.46(td,J＝7.5,1.5Hz,2H),1.61(d,J＝13.0Hz,2H),1.46(dd,J＝14.5,7.3Hz,2H),1.42–1.33(m,10H),0.94(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 9.68 (t, J=1.5Hz, 1H), 3.91 (d, J=12.0Hz, 2H), 2.65 (m, 2H), 2.46 (td, J= 7.5, 1.5Hz, 2H), 1.61 (d, J=13.0Hz, 2H), 1.46 (dd, J=14.5, 7.3Hz, 2H), 1.42–1.33 (m, 10H), 0.94 (m, 2H).
步骤3：4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯的制备Step 3: Preparation of benzyl 4-((3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000964
Figure PCTCN2022088560-appb-000964
把4-(3-丙醛)哌啶-1-羧酸叔丁酯(200mg,0.82mmol)和4-(甲基氨基)哌啶-1-羧酸苄酯(205mg,0.82mmol)溶于四氢呋喃(4mL)中，然后加入三乙酰氧基硼氢化钠(525mg,2.48mmol)，反应液室温搅拌过夜。用水(40mL)稀释，乙酸乙酯(30mL×3)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(EA:PE＝0-3:7)纯化得到白色油状物4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯。Dissolve tert-butyl 4-(3-propanal)piperidine-1-carboxylate (200 mg, 0.82 mmol) and benzyl 4-(methylamino)piperidine-1-carboxylate (205 mg, 0.82 mmol) In tetrahydrofuran (4 mL), sodium triacetoxyborohydride (525 mg, 2.48 mmol) was added, and the reaction solution was stirred at room temperature overnight. It was diluted with water (40 mL), extracted with ethyl acetate (30 mL×3), dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by column chromatography (EA:PE=0-3:7) to obtain a white oil 4-( Benzyl (3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝474.3. LC-MS: (ESI, m/z): [M+H] + = 474.3.
步骤4：4-(甲基(3-(哌啶-4-基)丙基)氨基)哌啶-1-羧酸苄酯的制备Step 4: Preparation of benzyl 4-(methyl(3-(piperidin-4-yl)propyl)amino)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000965
Figure PCTCN2022088560-appb-000965
把4-((3-(1-(叔丁氧羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯(90mg,0.19mmol)溶于DCM(5mL)中,然后三氟乙酸(0.5mL)加入,反应液在室温下搅拌1个小时，直接减压浓缩得到油状物4-(甲基(3-(哌啶-4-基)丙基)氨基)哌啶-1-羧酸苄酯。Benzyl 4-((3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propyl)(methyl)amino)piperidine-1-carboxylate (90 mg, 0.19 mmol) was dissolved in DCM (5 mL), then trifluoroacetic acid (0.5 mL) was added, the reaction solution was stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain 4-(methyl(3-(piperidin-4-yl)propyl) as an oily product ) amino) benzyl piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝374.1. LC-MS: (ESI, m/z): [M+H] + = 374.1.
步骤5：4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯的制备Step 5: 4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoro Methyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl) Preparation of benzyl)amino)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000966
Figure PCTCN2022088560-appb-000966
把(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(110mg,0.18mmol)和4-(甲基(3-(哌啶-4-基)丙基)氨基)哌啶-1-羧酸苄酯(三氟乙酸盐,90mg,0.18mmol)溶于DMF(3mL)中，HATU(83mg,0.22mmol)和DIEA(70mg,0.54mmol)加入，反应液室温搅拌过夜，用水(30mL)稀释，乙酸乙酯(30mL×3)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(MeOH:DCM＝0-1:9)纯化得到4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯。(1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (110 mg, 0.18 mmol) and 4-(methyl(3-(piperidin-4-yl)propane) benzyl)amino)piperidine-1-carboxylate (trifluoroacetate, 90 mg, 0.18 mmol) was dissolved in DMF (3 mL), HATU (83 mg, 0.22 mmol) and DIEA (70 mg, 0.54 mmol) were added, The reaction solution was stirred at room temperature overnight, diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by column chromatography (MeOH:DCM=0-1:9) to obtain 4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl)amino ) benzyl piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝958.2. LC-MS: (ESI, m/z): [M+H] + = 958.2.
步骤6：(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 6: (3-((R)-1-((7-Methoxy-2-methyl-6-((1R,4R)-4-(4-(3-(methyl(piperidine- 4-yl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester preparation
Figure PCTCN2022088560-appb-000967
Figure PCTCN2022088560-appb-000967
把4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羧酸苄酯(100mg,0.1mmol)溶于MeOH(5mL)中，加入Pd/C(20mg)，置换3次氢气，在氢气保护下室温搅拌1小时。过滤，滤饼用甲醇(5mL×3)洗涤，滤液减压浓缩得到(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl) Amino)piperidine-1-carboxylate benzyl ester (100 mg, 0.1 mmol) was dissolved in MeOH (5 mL), Pd/C (20 mg) was added, hydrogen was replaced three times, and the mixture was stirred at room temperature for 1 hour under the protection of hydrogen. Filtration, the filter cake was washed with methanol (5 mL×3), and the filtrate was concentrated under reduced pressure to obtain (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)- 4-(4-(3-(Methyl(piperidin-4-yl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5- (Trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝824.1. LC-MS: (ESI, m/z): [M+H] + = 824.1.
步骤7：(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 7: (3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-chloro-3-(2,4-dioxo) substituted tetrahydropyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2 - Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000968
Figure PCTCN2022088560-appb-000968
把化合物(3-((R)-1-((7-甲氧基-2-甲基-6-((1R,4R)-4-(4-(3-(甲基(哌啶-4-基)氨基)丙基)哌啶-1-羰基)环己基)喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(75mg,0.09mmol)和4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(39mg,0.09mmol)溶于DMSO(2mL)中，DIEA(35mg,0.27mmol)加入，反应液室温搅拌过夜。用水(20mL)稀释，乙酸乙酯(30mL×2)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(MeOH:DCM＝0-5:95)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。The compound (3-((R)-1-((7-methoxy-2-methyl-6-((1R,4R)-4-(4-(3-(methyl(piperidine-4 -yl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (75mg , 0.09 mmol) and pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (39 mg, 0.09 mmol) were dissolved in DMSO (2 mL), DIEA (35 mg, 0.27 mmol) was added and the reaction was stirred at room temperature overnight. Diluted with water (20 mL), extracted with ethyl acetate (30 mL×2), dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by column chromatography (MeOH:DCM=0-5:95) to give (3-((R )-1-((6-((1R,4R)-4-(4-(3-((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H)) -yl)benzoyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazoline-4- (yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1074.3. LC-MS: (ESI, m/z): [M+H] + = 1074.3.
步骤8：1-(5-(4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 8: 1-(5-(4-((3-(1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)(methyl) Preparation of amino)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000969
Figure PCTCN2022088560-appb-000969
将(3-((R)-1-((6-((1R,4R)-4-(4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)(甲基)氨基)丙基)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(40mg,0.04mmol)溶于二氯甲烷(3mL)中，然后加入三氟乙酸(0.3mL)，室温搅拌1个小时，直接减压浓缩，用饱和碳酸氢钠水溶液调pH到8-9，二氯甲烷(20mL×3)萃取，无水硫酸钠干燥，过滤，浓缩，粗品使用prep-HPLC纯化得到1-(5-(4-((3-(1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)(甲基)氨基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((R)-1-((6-((1R,4R)-4-(4-(3-(((1-(4-chloro-3-(2,4-dioxotetra) Hydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)(methyl)amino)propyl)piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (40 mg, 0.04 mmol) was dissolved in dichloromethane (3 mL), followed by trifluoromethyl Fluoroacetic acid (0.3 mL) was stirred at room temperature for 1 hour, directly concentrated under reduced pressure, adjusted to pH 8-9 with saturated aqueous sodium bicarbonate solution, extracted with dichloromethane (20 mL×3), dried over anhydrous sodium sulfate, filtered and concentrated , the crude product was purified by prep-HPLC to give 1-(5-(4-((3-(1-((1R,4R)-4-(4-((((R)-1-(3-amino-5- (Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl )(methyl)amino)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝974.3. LC-MS: (ESI, m/z): [M+H] + = 974.3.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.15–8.02(m,2H),7.63(d,J＝8.2Hz,1H),7.56(d,J＝1.9Hz,1H),7.40(d,J＝8.2Hz,1H),6.99(s,1H),6.86(d,J＝10.8Hz,2H),6.70(s,1H),5.64–5.47(m,3H),4.54-4.48(m,2H),3.96-3.88(m,4H),3.88-3.80(m,1H),3.80-3.74(m,2H),3.05-2.95(m,3H),2.91-2.85(m,2H),2.40-2.30(m,6H),2.15(s,3H),1.91-1.42(m,23H),1.25-1.15(m,2H),1.06–0.84(m,2H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s,1H),8.15-8.02(m,2H),7.63(d,J=8.2Hz,1H),7.56(d,J=1.9Hz, 1H), 7.40(d, J=8.2Hz, 1H), 6.99(s, 1H), 6.86(d, J=10.8Hz, 2H), 6.70(s, 1H), 5.64–5.47(m, 3H), 4.54-4.48(m, 2H), 3.96-3.88(m, 4H), 3.88-3.80(m, 1H), 3.80-3.74(m, 2H), 3.05-2.95(m, 3H), 2.91-2.85(m ,2H),2.40-2.30(m,6H),2.15(s,3H),1.91-1.42(m,23H),1.25-1.15(m,2H),1.06-0.84(m,2H).
实施例64：1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 64: 1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine -1-Carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 1: Preparation of methyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000970
Figure PCTCN2022088560-appb-000970
将6-溴-7-甲氧基-2-甲基喹唑啉-4-醇(6.2g,23.22mmol)加入到Pd(dppf)Cl 2(850mg,1.16mmol)，碳酸钠(4.9g,46.44mmol)和4-(4,4,5,5-四甲基-1,3-二氧戊烷-2-基)环己-3-烯-1-羧酸叔丁酯(8.1g,30.19mmol)的DMF/H 2O(80mL/8mL)混合溶液中，室温下搅拌过夜，待反应完全后，加水(800mL)稀释，用乙酸乙酯(200mL×5)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩。粗品使用柱层析(PE:EA＝1:100)纯化得到4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 6-Bromo-7-methoxy-2-methylquinazolin-4-ol (6.2 g, 23.22 mmol) was added to Pd(dppf)Cl 2 (850 mg, 1.16 mmol), sodium carbonate (4.9 g, 46.44 mmol) and tert-butyl 4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)cyclohex-3-ene-1-carboxylate (8.1 g, 30.19 mmol) in DMF/H 2 O (80 mL/8 mL) mixed solution, stirred overnight at room temperature, after the reaction was complete, diluted with water (800 mL), extracted with ethyl acetate (200 mL×5), washed with saturated brine, no Dry over sodium sulfate and concentrate under reduced pressure. The crude product was purified by column chromatography (PE:EA=1:100) to give 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1- Methyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝329.0. LC-MS: (ESI, m/z): [M+H] + = 329.0.
步骤2：4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 2: 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Preparation of methyl-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000971
Figure PCTCN2022088560-appb-000971
将4-(4-羟基-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(600mg,1.82mmol)加入到DBU(820mg,5.37mmol)和BOP(1.19g,2.69mmol)的DMF(10mL)溶液中，先室温下搅拌30min，(R)-(3-(1-氨基乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(600mg,1.97mmol)加入，反应液70℃下搅拌过夜。用水(100mL)稀释，析出固体，过滤，水洗三次，固体用二氯甲烷(100mL)溶解，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝1:1)纯化得到4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。Methyl 4-(4-hydroxy-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate (600 mg, 1.82 mmol) was added to DBU (820 mg , 5.37 mmol) and BOP (1.19 g, 2.69 mmol) in DMF (10 mL) solution, first stirred at room temperature for 30 min, (R)-(3-(1-aminoethyl)-5-(trifluoromethyl) Phenyl)carboxylate tert-butyl ester (600 mg, 1.97 mmol) was added, and the reaction solution was stirred at 70°C overnight. Diluted with water (100 mL), a solid was precipitated, filtered, washed with water three times, the solid was dissolved in dichloromethane (100 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:1) to obtain 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝615.2. LC-MS: (ESI, m/z): [M+H] + = 615.2.
步骤3：4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸的制备Step 3: 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy Preparation of yl-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid
Figure PCTCN2022088560-appb-000972
Figure PCTCN2022088560-appb-000972
将4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(1.1g,1.79mmol)加到氢氧化锂(430mg,17.9mmol)的THF/H 2O(20mL/10mL)溶液中，氮气保护，50℃下搅拌过夜，在冰浴下，缓慢滴加10％柠檬酸，将溶液调至弱酸性或中性，用乙酸乙酯(100mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，得到粗产品4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸。 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- Methyl 2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate (1.1 g, 1.79 mmol) was added to lithium hydroxide (430 mg, 17.9 mmol) in THF/H 2 O ( 20mL/10mL) solution under nitrogen protection, stirred overnight at 50°C, slowly added dropwise 10% citric acid under ice bath, adjusted the solution to weakly acidic or neutral, extracted with ethyl acetate (100mL×4), Washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain crude product 4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝601.2. LC-MS: (ESI, m/z): [M+H] + = 601.2.
步骤4：(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备Step 4: (3-((1R)-1-((6-(4-(4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine-1 (2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2 - Preparation of tert-butyl methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate
Figure PCTCN2022088560-appb-000973
Figure PCTCN2022088560-appb-000973
将4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羧酸(130mg,0.22mmol)，HATU(100mg,0.26mmol)和DIEA(85mg,0.66mmol)加入到1-(2-氯- 5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(140mg,0.23mmol)的DMF(10mL)溶液中，室温搅拌2小时，加入水(100mL)，析出固体，过滤，水洗3次，用二氯甲烷溶解，无水硫酸钠干燥，减压浓缩，得到粗产品(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy- 2-Methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylic acid (130 mg, 0.22 mmol), HATU (100 mg, 0.26 mmol) and DIEA (85 mg, 0.66 mmol) were added to 1-( 2-Chloro-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H) -diketone (140 mg, 0.23 mmol) in DMF (10 mL) solution, stirred at room temperature for 2 hours, added water (100 mL), precipitated a solid, filtered, washed with water 3 times, dissolved in dichloromethane, dried over anhydrous sodium sulfate, reduced Concentrated under pressure to give crude product (3-((1R)-1-((6-(4-(4-(2-((1-(4-chloro-3-(2,4-dioxotetrahydro) Pyrimidine-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy tert-butyl-2-methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝1059.5. LC-MS: (ESI, m/z): [M+H] + = 1059.5.
步骤5：1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl) )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-en-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine- Preparation of 1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000974
Figure PCTCN2022088560-appb-000974
将(3-((1R)-1-((6-(4-(4-(2-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)环己-1-烯-1-基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(190mg,0.18mmol)用二氯甲烷(5mL)溶解，加入三氟乙酸(1mL)，反应液室温搅拌2小时，减压浓缩，粗品使用反相制备纯化得到1-(5-(4-((2-(1-(4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己-3-烯-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(3-((1R)-1-((6-(4-(4-(2-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine-1(2H )-yl)benzoyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)cyclohex-1-en-1-yl)-7-methoxy-2-methyl tert-butyl quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate (190 mg, 0.18 mmol) was dissolved in dichloromethane (5 mL) and trifluoroacetic acid was added (1 mL), the reaction solution was stirred at room temperature for 2 hours, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(4-((2-(1-(4-(4-((((R)-1) -(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohex-3-ene-1- Carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝959.2. LC-MS: (ESI, m/z): [M+H] + = 959.2.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.19(s,1H),8.07(s,1H),7.63(d,J＝8.3Hz,1H),7.54(d,J＝1.8Hz,1H),7.38(dd,J＝8.2,1.8Hz,1H),6.99(s,1H),6.89(s,1H),6.85(s,1H),6.69(s,1H),5.83(s,1H),5.61-5.43(m,3H),4.51-4.37(m,2H),4.00-3.90(m,1H),3.85(s,3H),3.80-3.70(m,1H),3.67-3.52(m,2H),3.41(t,J＝6.3Hz,2H),3.24(d,J＝6.4Hz,2H),3.12-2.97(m,2H),2.92-2.70(m,4H),2.42-2.16(m,7H),1.90-1.56(m,8H),1.56-1.41(m,5H),1.21-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.50(s, 1H), 8.19(s, 1H), 8.07(s, 1H), 7.63(d, J=8.3Hz, 1H), 7.54(d, J=1.8Hz, 1H), 7.38(dd, J=8.2, 1.8Hz, 1H), 6.99(s, 1H), 6.89(s, 1H), 6.85(s, 1H), 6.69(s, 1H), 5.83(s, 1H), 5.61-5.43(m, 3H), 4.51-4.37(m, 2H), 4.00-3.90(m, 1H), 3.85(s, 3H), 3.80-3.70(m, 1H), 3.67-3.52(m, 2H), 3.41(t, J=6.3Hz, 2H), 3.24(d, J=6.4Hz, 2H), 3.12-2.97(m, 2H), 2.92-2.70(m, 4H) ,2.42-2.16(m,7H),1.90-1.56(m,8H),1.56-1.41(m,5H),1.21-0.90(m,4H).
实施例65：1-(2-氯-5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 65: 1-(2-Chloro-5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Carbonyl)piperidin-4-yl)methoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-((吡啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-((pyridin-4-ylmethoxy)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000975
Figure PCTCN2022088560-appb-000975
将4-(羟基甲基)哌啶-1-羧酸叔丁酯(1.0g,4.65mmol)溶于THF(40mL)溶液中，0℃下加入NaH(744mg,18.6mmol,60％)，搅拌2h，然后加入4-(溴甲基)吡啶(795mg,4.65mmol)，反应液室温继续搅拌2h，用水(100mL)稀释，乙酸乙酯(100mL×2)萃取，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(乙酸乙酯:石油醚＝1:0)纯化得到4-((吡啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯。4-(Hydroxymethyl)piperidine-1-carboxylate tert-butyl ester (1.0 g, 4.65 mmol) was dissolved in THF (40 mL) solution, NaH (744 mg, 18.6 mmol, 60%) was added at 0°C, and stirred 2h, then 4-(bromomethyl)pyridine (795mg, 4.65mmol) was added, the reaction solution was stirred at room temperature for 2h, diluted with water (100mL), extracted with ethyl acetate (100mL×2), dried over anhydrous sodium sulfate, filtered, It was concentrated under reduced pressure, and the crude product was purified by column chromatography (ethyl acetate:petroleum ether=1:0) to obtain tert-butyl 4-((pyridin-4-ylmethoxy)methyl)piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+Na] +＝329.1. LC-MS: (ESI, m/z): [M+Na] + = 329.1.
步骤2：4-((哌啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯的制备Step 2: Preparation of tert-butyl 4-((piperidin-4-ylmethoxy)methyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000976
Figure PCTCN2022088560-appb-000976
将4-((吡啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯(300mg,0.98mmol)溶于i-PrOH/H 2O(6:7,26mL)溶液中，氢气氛围下，加入Pd(OH)/C(100mg,20％)，反应液在75℃搅拌过夜，硅藻土过滤，滤液直接减压浓缩得到4-((哌啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯。 4-((Pyridin-4-ylmethoxy)methyl)piperidine-1-carboxylate tert-butyl ester (300 mg, 0.98 mmol) was dissolved in i-PrOH/H 2 O (6:7, 26 mL) solution , Pd(OH)/C (100 mg, 20%) was added under a hydrogen atmosphere, the reaction solution was stirred at 75°C overnight, filtered through celite, and the filtrate was directly concentrated under reduced pressure to obtain 4-((piperidin-4-ylmethane oxy)methyl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝313.2. LC-MS: (ESI, m/z): [M+H] + = 313.2.
步骤3：4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基)哌啶-1-羧酸叔丁酯的制备Step 3: 4-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy ) Preparation of methyl) piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000977
Figure PCTCN2022088560-appb-000977
将4-((哌啶-4-基甲氧基)甲基)哌啶-1-羧酸叔丁酯(120mg,0.38mmol)和DIEA(147mg,1.14mmol)加入到DMSO(10mL)中，然后加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(165mg,0.38mmol)，反应液室温搅拌30min，用水(40mL)稀释，乙酸乙酯(40mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝10:1)纯化得到4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基)哌啶-1-羧酸叔丁酯。4-((Piperidin-4-ylmethoxy)methyl)piperidine-1-carboxylate tert-butyl ester (120 mg, 0.38 mmol) and DIEA (147 mg, 1.14 mmol) were added to DMSO (10 mL), Then, pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (165 mg, 0.38 mmol) was added, and the reaction solution was stirred at room temperature for 30 min, followed by water (40 mL) Diluted, extracted with ethyl acetate (40 mL×3), the organic phase was washed with saturated brine (40 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=10:1) to obtain 4 -(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)methyl) tert-Butyl piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+NH 4] +＝580.2. LC-MS: (ESI, m/z): [M+NH 4 ] + = 580.2.
步骤4：1-(2-氯-5-(4-((哌啶-4-基甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(2-Chloro-5-(4-((piperidin-4-ylmethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H, Preparation of 3H)-dione
Figure PCTCN2022088560-appb-000978
Figure PCTCN2022088560-appb-000978
将4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基)哌啶-1-羧酸叔丁酯(80mg,0.14mmol)用二氯甲烷(5mL)溶解，加入氯化氢二氧六环溶液(4M,2mL)，反应液室温搅拌3小时，直接减压浓缩得到1-(2-氯-5-(4-((哌啶-4-基甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)methane base) piperidine-1-carboxylate tert-butyl ester (80 mg, 0.14 mmol) was dissolved in dichloromethane (5 mL), hydrogen chloride dioxane solution (4 M, 2 mL) was added, the reaction solution was stirred at room temperature for 3 hours, and the pressure was reduced directly. Concentration gave 1-(2-chloro-5-(4-((piperidin-4-ylmethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H )-diketone.
LC-MS:(ESI,m/z):[M+H] +＝463.1. LC-MS: (ESI, m/z): [M+H] + = 463.1.
步骤5：1-(2-氯-5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 5: 1-(2-Chloro-5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6- ((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl ) preparation of piperidin-4-yl)methoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000979
Figure PCTCN2022088560-appb-000979
(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(65mg,0.11mmol)用DMF(5mL)溶解，HATU(50mg,0.13mmol)，DIEA(50mg,0.39mmol)和1-(2-氯-5-(4-((哌啶-4-基甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(60mg,0.13mmol)分别加入，反应液室温搅拌30min，用水(20mL)稀释，乙酸乙酯(20mL×3)萃取，有机相用饱和食盐水(20mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。(1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl ) amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (65 mg, 0.11 mmol) was dissolved in DMF (5 mL), HATU (50 mg, 0.13 mmol) , DIEA (50 mg, 0.39 mmol) and 1-(2-chloro-5-(4-((piperidin-4-ylmethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine- 2,4(1H,3H)-dione (60 mg, 0.13 mmol) was added separately, the reaction solution was stirred at room temperature for 30 min, diluted with water (20 mL), extracted with ethyl acetate (20 mL×3), and the organic phase was washed with saturated brine (20 mL). ), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by prep-HPLC to obtain 1-(2-chloro-5-(4-(((1-((1R,4R)-4-(4-( ((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2- Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1037.4. LC-MS: (ESI, m/z): [M+H] + = 1037.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.31(d,J＝8.1Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.8Hz,1H),7.47-7.29(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.02-5.90(m,1H),4.52-4.32(m,2H),3.98-3.91(m,1H),3.89(s,3H),3.80-3.69(m,1H),3.66-3.54(m,2H),3.28-3.17(m,4H),3.15-3.09(m,2H),3.09-2.89(m,3H),2.84-2.69(m,3H),2.69-2.60(m,2H),2.42(s,3H),2.01(s,6H),1.91-1.46(m,17H),1.20-0.89(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.31 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.63 (d, J=8.2 Hz, 1H) ,7.54(d,J＝1.8Hz,1H),7.47-7.29(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.02-5.90(m,1H) ), 4.52-4.32(m, 2H), 3.98-3.91(m, 1H), 3.89(s, 3H), 3.80-3.69(m, 1H), 3.66-3.54(m, 2H), 3.28-3.17(m ,4H),3.15-3.09(m,2H),3.09-2.89(m,3H),2.84-2.69(m,3H),2.69-2.60(m,2H),2.42(s,3H),2.01(s ,6H),1.91-1.46(m,17H),1.20-0.89(m,4H).
实施例66：1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7- 甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 66: 1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-dioxide-2, 3-Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidine- 4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000980
Figure PCTCN2022088560-appb-000980
将1-(5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(120mg,0.24mmol)和(1R,4R)-4-(4-(((R)-1-(1,1-dioxido二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(120mg,0.24mmol)用DMF(3mL)溶解，HATU(108mg，0.28mmol)和DIEA(90mg,0.71mmol)加入，反应液室温搅拌1小时。用水(30mL)稀释，乙酸乙酯萃取(30mL×3)，合并有机相并用饱和食盐水洗，无水硫酸钠干燥，过滤，浓缩，粗品使用prep-HPLC纯化得到1-(5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-二氧化物-2,3-二氢苯并[b]噻吩-4-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)-2-(三氟甲基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine -2,4(1H,3H)-dione (120mg, 0.24mmol) and (1R,4R)-4-(4-(((R)-1-(1,1-dioxidodioxide-2, 3-Dihydrobenzo[b]thiophen-4-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (120 mg, 0.24 mmol) was dissolved in DMF (3 mL), HATU (108 mg, 0.28 mmol) and DIEA (90 mg, 0.71 mmol) were added, and the reaction solution was stirred at room temperature for 1 hour. Diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), combined the organic phases and washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was purified by prep-HPLC to obtain 1-(5-(4-( (2-(1-((1R,4R)-4-(4-(((R)-1-(1,1-dioxide-2,3-dihydrobenzo[b]thiophene-4- (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine -1-Carbonyl)-2-(trifluoromethyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1002.4. LC-MS: (ESI, m/z): [M+H] + = 1002.4.
1H NMR(400MHz,DMSO-d 6)δ10.53(s,1H),8.27(d,J＝7.2Hz,1H),8.06(s,1H),7.87(d,J＝8.2Hz,1H),7.80(d,J＝7.1Hz,1H),7.70(s,1H),7.59(t,J＝6.6Hz,2H),7.53(t,J＝7.6Hz,1H),6.98(s,1H),5.58(t,J＝7.0Hz,1H),4.57–4.33(m,2H),3.99–3.84(m,5H),3.81–3.70(m,1H),3.68–3.60(m,2H),3.52-3.40(m,5H),3.24(d,J＝6.2Hz,2H),3.14–2.89(m,3H),2.85-2.65(m,4H),2.32(s,3H),1.92–1.40(m,20H),1.23–0.89(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.53(s, 1H), 8.27(d, J=7.2Hz, 1H), 8.06(s, 1H), 7.87(d, J=8.2Hz, 1H) ,7.80(d,J＝7.1Hz,1H),7.70(s,1H),7.59(t,J＝6.6Hz,2H),7.53(t,J＝7.6Hz,1H),6.98(s,1H) ,5.58(t,J＝7.0Hz,1H),4.57-4.33(m,2H),3.99-3.84(m,5H),3.81-3.70(m,1H),3.68-3.60(m,2H),3.52 -3.40(m, 5H), 3.24(d, J=6.2Hz, 2H), 3.14-2.89(m, 3H), 2.85-2.65(m, 4H), 2.32(s, 3H), 1.92-1.40(m ,20H),1.23–0.89(m,4H).
实施例67：1-(2-氯-5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 67: 1-(2-Chloro-5-(4-((2-(4-((1R,4R)-4-(4-((((R)-1-(4-(2-Chloro) -6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000981
Figure PCTCN2022088560-appb-000981
将1-(2-氯-5-(4-((2-(哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(150mg,粗品)溶于DMF(5mL)，(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(94mg,0.22mmol)，HATU(107mg,0.28mmol)和DIEA(145mg,1.1mmol)分别加入，室温搅拌2小时，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)萃取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(2-氯-5-(4-((2-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(4-((2-(piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione (150 mg, crude) was dissolved in DMF (5 mL), (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-(( Dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid ( 94mg, 0.22mmol), HATU (107mg, 0.28mmol) and DIEA (145mg, 1.1mmol) were added separately, stirred at room temperature for 2 hours, added water (50mL) and stirred for 5 minutes, extracted with ethyl acetate (30mLx3), saturated brine (50 mL) washed the organic phase, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by reverse-phase preparation to obtain 1-(2-chloro-5-(4-((2-(4-((1R, 4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl ) dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1052.4. LC-MS: (ESI, m/z): [M+H] + = 1052.4.
1H NMR(400MHz,DMSO-d 6)δ10.48(s,1H),8.29(d,J＝8.3Hz,1H),8.04(s,1H),7.62(d,J＝8.1Hz,1H),7.53(d,J＝1.6Hz,1H),7.45–7.31(m,4H),7.23(s,1H),7.02(s,1H),6.96(s,1H),5.96(t,J＝7.1Hz,1H),4.52–4.28(m,1H),3.89(s,3H),3.80–3.40(m,10H),3.26(d,J＝6.3Hz,2H),3.12(s,2H),2.97–2.88(m,1H),2.79–2.59(m,4H),2.45–2.39(m,5H),2.38–2.33(m,2H),2.01(s,6H),1.94–1.46(m,16H),1.13(d,J＝10.9Hz,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.48 (s, 1H), 8.29 (d, J=8.3 Hz, 1H), 8.04 (s, 1H), 7.62 (d, J=8.1 Hz, 1H) ,7.53(d,J=1.6Hz,1H),7.45–7.31(m,4H),7.23(s,1H),7.02(s,1H),6.96(s,1H),5.96(t,J=7.1 Hz, 1H), 4.52–4.28 (m, 1H), 3.89 (s, 3H), 3.80–3.40 (m, 10H), 3.26 (d, J=6.3Hz, 2H), 3.12 (s, 2H), 2.97 –2.88(m,1H), 2.79–2.59(m,4H), 2.45–2.39(m,5H), 2.38–2.33(m,2H), 2.01(s,6H), 1.94–1.46(m,16H) ,1.13(d,J=10.9Hz,2H).
实施例68：1-(2-氯-5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 68: 1-(2-Chloro-5-(4-(3-(4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羧酸叔丁酯的制备Step 1: Preparation of tert-butyl 4-(3-(piperidin-4-yloxy)propyl)piperazine-1-carboxylate
Figure PCTCN2022088560-appb-000982
Figure PCTCN2022088560-appb-000982
将4-(3-((1-((苄氧)羰基)哌啶-4-基)氧)丙基)哌嗪-1-羧酸叔丁酯(400mg,0.87mmol)和Pd/C(10％,100mg)用乙酸乙酯(10mL)溶解，反应液加热到70℃并搅拌3小时，过滤，固体用乙酸乙酯(10mL×3)洗三次，减压浓缩得到4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羧酸叔丁酯。4-(3-((1-((Benzyloxy)carbonyl)piperidin-4-yl)oxy)propyl)piperazine-1-carboxylate tert-butyl ester (400 mg, 0.87 mmol) and Pd/C ( 10%, 100 mg) was dissolved in ethyl acetate (10 mL), the reaction solution was heated to 70 °C and stirred for 3 hours, filtered, the solid was washed three times with ethyl acetate (10 mL×3), and concentrated under reduced pressure to obtain 4-(3-( Piperidin-4-yloxy)propyl)piperazine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝328.3. LC-MS: (ESI, m/z): [M+H] + = 328.3.
步骤2：4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧)丙基)哌嗪-1-羧酸叔丁酯的制备Step 2: 4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy ) Preparation of propyl)piperazine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000983
Figure PCTCN2022088560-appb-000983
将4-(3-(哌啶-4-基氧)丙基)哌嗪-1-羧酸叔丁酯(230mg,0.70mmol)用DMSO(10mL)溶解，4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(360mg,0.82mmol)和DIEA(271mg,2.10mmol)分别加入，室温搅拌过夜，用水(50mL)稀释，乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(PE:EA＝1:10)纯化得到4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧)丙基)哌嗪-1-羧酸叔丁酯。4-(3-(Piperidin-4-yloxy)propyl)piperazine-1-carboxylate tert-butyl ester (230 mg, 0.70 mmol) was dissolved in DMSO (10 mL), 4-chloro-3-(2, 4-Dioxotetrahydropyrimidin-1(2H)-yl)benzoic acid pentafluorophenyl ester (360 mg, 0.82 mmol) and DIEA (271 mg, 2.10 mmol) were added separately, stirred at room temperature overnight, diluted with water (50 mL), acetic acid Extracted with ethyl ester (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by column chromatography (PE:EA=1:10) to obtain 4-(3-((1-(4 - tert-butyl chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy)propyl)piperazine-1-carboxylate .
LC-MS:(ESI,m/z):[M+H] +＝578.3. LC-MS: (ESI, m/z): [M+H] + = 578.3.
步骤3：1-(2-氯-5-(4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-(3-(piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H, Preparation of 3H)-dione
Figure PCTCN2022088560-appb-000984
Figure PCTCN2022088560-appb-000984
将4-(3-((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)氧)丙基)哌嗪-1-羧酸叔丁酯(220mg,0.47mmol)用二氯甲烷(5mL)溶解，加入三氟乙酸(1mL)，反应液室温搅拌过夜，缓慢滴加饱和碳酸氢钠水溶液，将反应液pH值调至7-8，用二氯甲烷与异丙醇五比一混合溶液(25mL×4)萃取，无水硫酸钠干燥，过滤，减压浓缩得到1-(2-氯-5-(4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。4-(3-((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)oxy)propane (base) piperazine-1-carboxylate tert-butyl ester (220 mg, 0.47 mmol) was dissolved in dichloromethane (5 mL), trifluoroacetic acid (1 mL) was added, the reaction solution was stirred at room temperature overnight, and saturated aqueous sodium bicarbonate solution was slowly added dropwise, The pH value of the reaction solution was adjusted to 7-8, extracted with a five-to-one mixed solution of dichloromethane and isopropanol (25 mL×4), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 1-(2-chloro- 5-(4-(3-(Piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝478.2. LC-MS: (ESI, m/z): [M+H] + = 478.2.
步骤4：1-(2-氯-5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(2-Chloro-5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-Chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000985
Figure PCTCN2022088560-appb-000985
将1-(2-氯-5-(4-(3-(哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(90mg,0.19mmol)，HATU(87mg,0.23mmol)和DIEA(74mg,0.57mmol)分别加入到(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(106mg,0.19mmol)的DMF(10mL)溶液中，室温搅拌2小时，用水(100mL)稀释，析出固体，过滤，水洗3次，用二氯甲烷溶解固体，无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(2-氯-5-(4-(3-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丙氧基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1-(2-Chloro-5-(4-(3-(piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H) - Diketone (90mg, 0.19mmol), HATU (87mg, 0.23mmol) and DIEA (74mg, 0.57mmol) were added to (1R,4R)-4-(4-((((R)-1-(4- (2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl) A solution of cyclohexane-1-carboxylic acid (106 mg, 0.19 mmol) in DMF (10 mL) was stirred at room temperature for 2 hours, diluted with water (100 mL), a solid was precipitated, filtered, washed with water 3 times, and the solid was dissolved in dichloromethane. It was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by reverse-phase preparation to obtain 1-(2-chloro-5-(4-(3-(4-((1R,4R)-4-(4-(( (R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methyl quinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)propoxy)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H) - Diketones.
LC-MS:(ESI,m/z):[M+H] +＝1052.4. LC-MS: (ESI, m/z): [M+H] + = 1052.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.32(d,J＝7.7Hz,1H),8.05(s,1H),7.63(d,J＝8.3Hz,1H),7.57(s,1H),7.47–7.30(m,4H),7.24(s,1H),7.02(s,1H),6.97(s,1H),5.97(t,J＝7.2Hz,1H),4.00-3.84(s,4H),3.80-3.71(m,1H),3.66-3.57(m,1H),3.49-3.35(m,8H),3.20-3.07(m,3H),3.00-2.84(m,1H),2.78-2.58(m,3H),2.42(s,3H),2.40-2.26(m,6H),2.01(s,6H),1.92-1.75(m,6H),1.75–1.38(m,12H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.32(d, J=7.7Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.3Hz, 1H) ,7.57(s,1H),7.47–7.30(m,4H),7.24(s,1H),7.02(s,1H),6.97(s,1H),5.97(t,J=7.2Hz,1H), 4.00-3.84(s, 4H), 3.80-3.71(m, 1H), 3.66-3.57(m, 1H), 3.49-3.35(m, 8H), 3.20-3.07(m, 3H), 3.00-2.84(m ,1H),2.78-2.58(m,3H),2.42(s,3H),2.40-2.26(m,6H),2.01(s,6H),1.92-1.75(m,6H),1.75–1.38(m ,12H).
实施例69：1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 69: 1-(2-Chloro-5-(4-((2-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro) -6-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸叔丁酯的制备Step 1: (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl) Preparation of ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-000986
Figure PCTCN2022088560-appb-000986
将化合物(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-醛苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(450mg,0.78mmol)和甲胺(2M/THF溶液,7.8mmol)溶于二氯乙烷(10mL)中，三乙酰基硼氢化钠(496mg,2.34mmol)加入。反应液加热到80℃并搅拌1小时。直接减压浓缩，粗品使用柱层析(MeOH:DCM＝1:10,流速40ml/min)纯化得到(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸叔丁酯。Compound (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-aldehyde phenyl)thiophen-2-yl)ethyl)amino)-7-methyl Methyl oxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate (450 mg, 0.78 mmol) and methylamine (2M in THF, 7.8 mmol) were dissolved in dichloroethane ( 10 mL), sodium triacetylborohydride (496 mg, 2.34 mmol) was added. The reaction solution was heated to 80°C and stirred for 1 hour. Directly concentrated under reduced pressure, the crude product was purified by column chromatography (MeOH:DCM=1:10, flow rate 40ml/min) to obtain (1R,4R)-4-(4-((((R)-1-(4-(2) -Chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane - 1-Carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝593.3. LC-MS: (ESI, m/z): [M+H] + = 593.3.
步骤2：(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 2: (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl) Preparation of ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000987
Figure PCTCN2022088560-appb-000987
将(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸叔丁酯(300mg,0.5mmol)和氢氧化锂(60mg,2.5mmol)用混合溶液(MeOH/H 2O＝10/1,5mL)溶解。反应液加热到70℃并搅拌2小时。冷却，使用1M HCl将反应液pH值调到3～4，再使用饱和碳酸氢钠水溶液将反应液pH值调到7～8，使用乙酸乙酯(100mL×3)萃取，合并有机相，饱和食盐水洗，无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相(ACN:H 2O＝1:1)纯化得到(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸。 (1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl ) amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylate tert-butyl ester (300 mg, 0.5 mmol) and lithium hydroxide (60 mg, 2.5 mmol) were used The mixed solution (MeOH/H 2 O=10/1, 5 mL) was dissolved. The reaction solution was heated to 70°C and stirred for 2 hours. Cool, adjust the pH of the reaction solution to 3-4 with 1M HCl, adjust the pH of the reaction solution to 7-8 with saturated aqueous sodium bicarbonate solution, extract with ethyl acetate (100 mL×3), combine the organic phases, saturated Washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was purified by reverse phase (ACN:H 2 O=1:1) to obtain (1R,4R)-4-(4-(((R)-1) -(4-(2-Chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6 - base) cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝579.2. LC-MS: (ESI, m/z): [M+H] + = 579.2.
步骤3：1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro- 6-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000988
Figure PCTCN2022088560-appb-000988
将(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(80mg,0.14mmol)用DMF(5mL)溶解，HATU(65mg,0.17mmol)，1-(2-氯-5-(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(80mg,0.17mmol)和DIEA(54mg,0.42mmol)加入，反应液室温搅拌1小时，用水(20mL)稀释，乙酸乙酯(20mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，过滤，减压浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-((2-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)乙氧基)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。(1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl )amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (80 mg, 0.14 mmol) was dissolved in DMF (5 mL), HATU (65 mg, 0.17 mmol) , 1-(2-chloro-5-(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4( 1H,3H)-dione (80 mg, 0.17 mmol) and DIEA (54 mg, 0.42 mmol) were added, the reaction solution was stirred at room temperature for 1 hour, diluted with water (20 mL), extracted with ethyl acetate (20 mL×3), and the organic phase was saturated with Washed with brine (40 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was purified by prep-HPLC to obtain 1-(2-chloro-5-(4-((2-(1-((1R,4R )-4-(4-(((R)-1-(4-(2-chloro-6-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)ethoxy)methyl)piperidine-1-carbonyl)phenyl)di Hydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1037.4. LC-MS: (ESI, m/z): [M+H] + = 1037.4.
1H NMR(400MHz,DMSO-d 6)δ10.50(s,1H),8.32(d,J＝8.3Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.7Hz,1H),7.45(d,J＝7.5Hz,1H),7.42–7.30(m,3H),7.28(s,1H),7.02(s,1H),6.98(s,1H),6.07–5.86(m,1H),4.38(d,J＝12.6Hz,2H),3.89(s,4H),3.73(d,J＝7.1Hz,1H),3.66–3.51(m,2H),3.44–3.36(m,4H),3.23(d,J＝6.2Hz,2H),3.11–2.88(m,3H),2.78–2.59(m,4H),2.42(s,3H),2.12(s,3H),1.92–1.39(m,21H),1.18–0.87(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.50(s, 1H), 8.32(d, J=8.3Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝1.7Hz,1H),7.45(d,J＝7.5Hz,1H),7.42–7.30(m,3H),7.28(s,1H),7.02(s,1H),6.98( s, 1H), 6.07–5.86 (m, 1H), 4.38 (d, J=12.6Hz, 2H), 3.89 (s, 4H), 3.73 (d, J=7.1Hz, 1H), 3.66–3.51 (m ,2H),3.44–3.36(m,4H),3.23(d,J=6.2Hz,2H),3.11–2.88(m,3H),2.78–2.59(m,4H),2.42(s,3H), 2.12(s,3H),1.92–1.39(m,21H),1.18–0.87(m,4H).
实施例70：1-(2-氯-5-(4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 70: 1-(2-Chloro-5-(4-(2-((1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro) -6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane- 1-Carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methan) (yl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl) Preparation of tert-butyl methoxy)ethyl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000989
Figure PCTCN2022088560-appb-000989
将(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(80mg,0.13mmol)，HATU(62mg,0.16mmol)和DIEA(50mg,0.39mmol)加入到4-(2-(哌啶-4-基甲氧基)乙基)哌啶-1-羧酸叔丁酯(43mg,0.13mmol)的DMF(5mL)溶液中，室温搅拌1小时,用水(50mL)稀释，析出固体，过滤，水洗3次，用二氯甲烷溶解固体，无水硫酸钠干燥，减压浓缩，粗品使用反相制备纯化得到4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯。(1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (80 mg, 0.13 mmol), HATU (62 mg, 0.16 mmol) and DIEA (50 mg, 0.39 mmol) was added to a solution of tert-butyl 4-(2-(piperidin-4-ylmethoxy)ethyl)piperidine-1-carboxylate (43 mg, 0.13 mmol) in DMF (5 mL) and stirred at room temperature 1 hour, diluted with water (50 mL), a solid was precipitated, filtered, washed with water 3 times, the solid was dissolved in dichloromethane, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 4-(2-((1 -((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl) Ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1 - tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝901.4. LC-MS: (ESI, m/z): [M+H] + = 901.4.
步骤2：((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)甲酮的制备Step 2: ((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophene-2- yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-((2-(piperidin-4-yl)ethoxy)methyl ) preparation of piperidin-1-yl)methanone
Figure PCTCN2022088560-appb-000990
Figure PCTCN2022088560-appb-000990
将4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羧酸叔丁酯(80mg，0.09mmol)加入到氯化氢的二氧六环(4M，2mL)溶液中，反应液室温搅拌1小时，直接减压浓缩得到粗品((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)甲酮。4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) Phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy tert-butyl) ethyl) piperidine-1-carboxylate (80 mg, 0.09 mmol) was added to a solution of hydrogen chloride in dioxane (4 M, 2 mL), the reaction solution was stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain the crude product ((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine -1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝801.3. LC-MS: (ESI, m/z): [M+H] + = 801.3.
步骤3：1-(2-氯-5-(4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 Preparation of -carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000991
Figure PCTCN2022088560-appb-000991
将((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((2-(哌啶-4-基)乙氧基)甲基)哌啶-1-基)甲酮(70mg,0.09mmol)加入到4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(39mg,0.08mmol)和DIEA(35mg,0.27mmol)的DMSO(5mL)溶液中，室温搅拌过夜，用水(50mL)稀释，乙酸乙酯(25mL×4)萃取，饱和食盐水洗，无水硫酸钠干燥，减压浓缩，粗品使用反相制备纯化得到1-(2-氯-5-(4-(2-((1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)乙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl) Ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-((2-(piperidin-4-yl)ethoxy)methyl)piperidine Iridin-1-yl)methanone (70 mg, 0.09 mmol) was added to pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (39 mg, 0.08 mmol) and DIEA (35 mg, 0.27 mmol) in DMSO (5 mL) solution, stirred at room temperature overnight, diluted with water (50 mL), extracted with ethyl acetate (25 mL×4), washed with saturated brine, dried over anhydrous sodium sulfate, reduced was concentrated under pressure, and the crude product was purified by reverse-phase preparation to give 1-(2-chloro-5-(4-(2-((1-((1R,4R)-4-(4-((((R)-1-() 4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazoline-6- yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)ethyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1051.5. LC-MS: (ESI, m/z): [M+H] + = 1051.5.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.30(d,J＝8.1Hz,1H),8.05(s,1H),7.62(d,J＝8.2Hz,1H),7.53(d,J＝2.0Hz,1H),7.45-7.31(m,4H),7.24(d,J＝1.3Hz,1H),7.02(s,1H),6.96(s,1H),6.03–5.89(m,1H),4.48-4.32(m,2H),3.97-3.85(m,4H),3.79-3.68(m,1H),3.66-3.52(m,2H),3.40(t,J＝6.4Hz,2H),3.21(d,J＝6.1Hz,2H),3.16–2.90(m,5H),2.82–2.52(m,7H),2.42(s,3H),2.01(s,6H),1.88–1.43(m,20H),1.19–0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.49 (s, 1H), 8.30 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.62 (d, J=8.2 Hz, 1H) ,7.53(d,J＝2.0Hz,1H),7.45-7.31(m,4H),7.24(d,J＝1.3Hz,1H),7.02(s,1H),6.96(s,1H),6.03– 5.89(m, 1H), 4.48-4.32(m, 2H), 3.97-3.85(m, 4H), 3.79-3.68(m, 1H), 3.66-3.52(m, 2H), 3.40(t, J=6.4 Hz, 2H), 3.21(d, J＝6.1Hz, 2H), 3.16-2.90(m, 5H), 2.82-2.52(m, 7H), 2.42(s, 3H), 2.01(s, 6H), 1.88 –1.43(m,20H),1.19–0.90(m,4H).
实施例71：1-(2-氯-5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 71: 1-(2-Chloro-5-(4-(4-(4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperazin-1-yl)butyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯的制备Step 1: 4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl) )phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butane Preparation of tert-butyl) piperidine-1-carboxylate
Figure PCTCN2022088560-appb-000992
Figure PCTCN2022088560-appb-000992
将(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(120mg,0.20mmol)，4-(4-(哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(66mg,0.20mmol)和HATU(91mg,0.24mmol)溶于DMF(3mL)中，加入DIEA(78mg,0.61mmol)，反应液室温搅拌1小时，用水(30mL)稀释，乙酸乙酯萃取(30mL×3)，合并有机相，饱和食盐水洗涤，无水硫酸钠干燥，过滤，浓缩，粗品使用柱层析(DCM:MeOH＝10:1)得到4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯。(1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (120 mg, 0.20 mmol), 4-(4-(piperazin-1-yl) ) butyl) piperidine-1-carboxylate tert-butyl ester (66 mg, 0.20 mmol) and HATU (91 mg, 0.24 mmol) were dissolved in DMF (3 mL), DIEA (78 mg, 0.61 mmol) was added, and the reaction solution was stirred at room temperature for 1 h, diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), combined the organic phases, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and the crude product was subjected to column chromatography (DCM:MeOH=10:1 ) to give 4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)) Phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl ) tert-butyl piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝900.6. LC-MS: (ESI, m/z): [M+H] + = 900.6.
步骤2：((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮的制备Step 2: ((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophene-2- yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazine-1 - preparation of ketone
Figure PCTCN2022088560-appb-000993
Figure PCTCN2022088560-appb-000993
将4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羧酸叔丁酯(149mg,0.17mmol)用氯化氢的1,4-二氧六环溶液(4M，5mL)溶解，室温搅拌1小时，直接减压浓缩得到((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮。4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)benzene (yl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)butyl) Piperidine-1-carboxylate tert-butyl ester (149 mg, 0.17 mmol) was dissolved in a solution of hydrogen chloride in 1,4-dioxane (4M, 5 mL), stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to give ((1R,4R )-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)- 7-Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazin-1-yl)methanone.
LC-MS:(ESI,m/z):[M+H] +＝800.4. LC-MS: (ESI, m/z): [M+H] + = 800.4.
步骤3：1-(2-氯-5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 3: 1-(2-Chloro-5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperazin-1-yl)butyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-000994
Figure PCTCN2022088560-appb-000994
将((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-(4-(哌啶-4-基)丁基)哌嗪-1-基)甲酮(158mg,0.11mmol)，4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(47mg,0.11mmol)溶于DMSO(2mL)中，搅拌下加入DIEA(42mg,0.32mmol)， 室温搅拌1小时。用水(30mL)稀释，乙酸乙酯萃取(30mL×3)，合并上有机相，饱和食盐水洗涤，无水硫酸钠干燥，过滤，减压浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-(4-(4-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)丁基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl) Ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-(4-(piperidin-4-yl)butyl)piperazin-1-yl ) ketone (158 mg, 0.11 mmol), pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (47 mg, 0.11 mmol) in DMSO (2 mL), DIEA (42 mg, 0.32 mmol) was added with stirring, and the mixture was stirred at room temperature for 1 hour. Diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), combined the organic phases, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by prep-HPLC to obtain 1-(2- Chloro-5-(4-(4-(4-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro-6-((dimethylamino)) Methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl )butyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1050.5. LC-MS: (ESI, m/z): [M+H] + = 1050.5.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.30(d,J＝7.7Hz,1H),8.05(s,1H),7.63(d,J＝8.3Hz,1H),7.54(s,1H),7.47–7.31(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.01–5.90(m,1H),4.50-4.42(m,1H),3.89(s,3H),3.80-3.68(m,1H),3.66-3.52(m,2H),3.50-3.40(m,4H),3.18-3.10(m,2H),3.02-2.90(m,2H),2.80-2.65(m,4H),2.42(s,3H),2.38-2.20(m,6H),2.01(s,6H),1.82-1.42(m,18H),1.30-1.22(m,4H),1.13-0.96(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.49(s, 1H), 8.30(d, J=7.7Hz, 1H), 8.05(s, 1H), 7.63(d, J=8.3Hz, 1H) ,7.54(s,1H),7.47–7.31(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.01–5.90(m,1H),4.50-4.42 (m,1H),3.89(s,3H),3.80-3.68(m,1H),3.66-3.52(m,2H),3.50-3.40(m,4H),3.18-3.10(m,2H),3.02 -2.90(m, 2H), 2.80-2.65(m, 4H), 2.42(s, 3H), 2.38-2.20(m, 6H), 2.01(s, 6H), 1.82-1.42(m, 18H), 1.30 -1.22(m,4H),1.13-0.96(m,2H).
实施例72：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 72: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5] Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(4-羟基-2,7-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯的制备Step 1: Preparation of methyl 4-(4-hydroxy-2,7-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate
Figure PCTCN2022088560-appb-000995
Figure PCTCN2022088560-appb-000995
6-溴-2,7-二甲基喹唑啉-4-醇(900mg,3.56mmol)用DMF/H 2O(22mL,10/1)溶解，加入4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)环己-3-烯-1-羧酸甲酯(1135mg,4.27mmol)，碳酸钠(755mg,7.12mmol)和Pd(dppf)Cl 2(264mg,0.36mmol)，在氮气保护下110℃搅拌过夜，加水(100mL)并搅拌5分钟，用乙酸乙酯(100mLx3)萃取，饱和食盐水(200mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9)纯化得到4-(4-羟基-2,7-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯。 6-Bromo-2,7-dimethylquinazolin-4-ol (900 mg, 3.56 mmol) was dissolved in DMF/H 2 O (22 mL, 10/1), 4-(4,4,5,5 was added - Tetramethyl-1,3,2-dioxaboropentan-2-yl)cyclohex-3-ene-1-carboxylic acid methyl ester (1135 mg, 4.27 mmol), sodium carbonate (755 mg, 7.12 mmol) and Pd(dppf)Cl 2 (264 mg, 0.36 mmol) was stirred at 110 °C overnight under nitrogen protection, water (100 mL) was added and stirred for 5 minutes, extracted with ethyl acetate (100 mL×3), and the organic phase was washed with saturated brine (200 mL), It was dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was purified by column chromatography (MeOH:DCM=1:9) to give 4-(4-hydroxy-2,7-methylquinazolin-6-yl) Methyl cyclohex-3-ene-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝313.1. LC-MS: (ESI, m/z): [M+H] + = 313.1.
步骤2：(1R,4R)-4-(4-羟基-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 2: Preparation of (1R,4R)-4-(4-hydroxy-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000996
Figure PCTCN2022088560-appb-000996
在的高压釜(100mL)中，加入4-(4-羟基-2,7-甲基喹唑啉-6-基)环己-3-烯-1-羧酸甲酯(380mg,1.22mmol)，用MeOH(30mL)溶解后，加入Pd(OH) 2/C(115mg,30％)，在氢气环境中(2MPa)于70℃反应48h，过滤，减压浓缩，粗品使用反相制备纯化得到(1R,4R)-4-(4-羟基-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸甲酯。 Into an autoclave (100 mL), add methyl 4-(4-hydroxy-2,7-methylquinazolin-6-yl)cyclohex-3-ene-1-carboxylate (380 mg, 1.22 mmol) , dissolved in MeOH (30 mL), added Pd(OH) 2 /C (115 mg, 30%), reacted at 70 °C for 48 h in a hydrogen atmosphere (2 MPa), filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation. (1R,4R)-4-(4-hydroxy-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝315.2. LC-MS: (ESI, m/z): [M+H] + = 315.2.
1H NMR(400MHz,DMSO)δ12.09(s,1H),8.15(s,1H),7.56(s,1H),3.92(s,3H),2.95(t,J＝11.6Hz,1H),2.43(s,3H),2.36(s,3H),2.35–2.24(m,1H),2.06(d,J＝10.7Hz,2H),1.90–1.84(m,2H),1.67–1.40(m,4H). 1 H NMR (400MHz, DMSO) δ 12.09(s, 1H), 8.15(s, 1H), 7.56(s, 1H), 3.92(s, 3H), 2.95(t, J=11.6Hz, 1H), 2.43(s, 3H), 2.36(s, 3H), 2.35-2.24(m, 1H), 2.06(d, J=10.7Hz, 2H), 1.90-1.84(m, 2H), 1.67-1.40(m, 4H).
步骤3：(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯的制备Step 3: (1R,4R)-4-(2,7-Dimethyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Preparation of amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester
Figure PCTCN2022088560-appb-000997
Figure PCTCN2022088560-appb-000997
将(1R,4R)-4-(4-羟基-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸甲酯(250mg,0.80mmol)溶于DMF(5mL)，加入BOP(506mg,1.19mmol)和DBU(303mg,1.99mmol)，室温搅拌0.5小时后，加入(R)-1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-胺(224mg,0.96mmol)，加热至70℃搅拌过夜，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mLx3)萃取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相纯化得到(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯。Methyl (1R,4R)-4-(4-hydroxy-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carboxylate (250 mg, 0.80 mmol) was dissolved in DMF (5 mL) ), BOP (506 mg, 1.19 mmol) and DBU (303 mg, 1.99 mmol) were added, and after stirring at room temperature for 0.5 h, (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl Alkan-1-amine (224 mg, 0.96 mmol), heated to 70 °C and stirred overnight, added water (50 mL) and stirred for 5 minutes, extracted with ethyl acetate (30 mL×3), washed the organic phase with saturated brine (50 mL), washed with anhydrous It was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by reverse phase to obtain (1R,4R)-4-(2,7-dimethyl-4-(((R)-1-(3-nitro-5). -(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester.
LC-MS:(ESI,m/z):[M+H] +＝531.3. LC-MS: (ESI, m/z): [M+H] + = 531.3.
步骤4：(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸的制备Step 4: (1R,4R)-4-(2,7-Dimethyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Preparation of amino)quinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000998
Figure PCTCN2022088560-appb-000998
将(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸甲酯(210mg,0.40mmol)溶于THF/H 2O(15mL,2:1)中，加入氢氧化锂(190mg,8.00mmol)，50℃搅拌过夜，加水(20mL)，用1M盐酸调节pH至6，用MeOH/DCM(1/9,30mL×3)萃取，经无水硫酸钠干燥，过滤，减压浓缩，得到(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸，直接用于下一步。 (1R,4R)-4-(2,7-Dimethyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) Quinazolin-6-yl)cyclohexane-1-carboxylate methyl ester (210 mg, 0.40 mmol) was dissolved in THF/H 2 O (15 mL, 2:1) and lithium hydroxide (190 mg, 8.00 mmol) was added , stirred at 50°C overnight, added water (20 mL), adjusted pH to 6 with 1M hydrochloric acid, extracted with MeOH/DCM (1/9, 30 mL×3), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give (1R ,4R)-4-(2,7-dimethyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline -6-yl)cyclohexane-1-carboxylic acid, used directly in the next step.
LC-MS:(ESI,m/z):[M+H] +＝517.4. LC-MS: (ESI, m/z): [M+H] + = 517.4.
步骤5：(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸的制备Step 5: (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethyl Preparation of quinazolin-6-yl)cyclohexane-1-carboxylic acid
Figure PCTCN2022088560-appb-000999
Figure PCTCN2022088560-appb-000999
将(1R,4R)-4-(2,7-二甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)环己烷-1-羧酸(150mg,0.29mmol)，溶于乙醇(10mL)，加入Raney-Ni(0.5mL)和N 2H 4-H 2O(85％,0.5mL)，室温反应0.5小时，过滤，减压浓缩，得到(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸。 (1R,4R)-4-(2,7-Dimethyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) Quinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.29 mmol), dissolved in ethanol (10 mL), added Raney-Ni (0.5 mL) and N2H4 - H2O (85% , 0.5 mL), reacted at room temperature for 0.5 hours, filtered and concentrated under reduced pressure to obtain (1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) yl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carboxylic acid.
LC-MS:(ESI,m/z):[M+H] +＝487.2. LC-MS: (ESI, m/z): [M+H] + = 487.2.
步骤6：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 6: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]deca Preparation of monoalkane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-001000
Figure PCTCN2022088560-appb-001000
将(1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羧酸(70mg,0.14mmol)溶于DMF(5mL)，加入1-(2-氯-5-(9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(84mg,0.17mmol)，DIEA(55mg,0.42mmol)和pyBOP(88mg,0.17mmol)，室温反应1h，加水(50mL)并搅拌5分钟，用乙酸乙酯(30mL×3)萃取，饱和食盐水(50mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相制备纯化得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2,7-二甲基喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethylquinoline oxazolin-6-yl)cyclohexane-1-carboxylic acid (70 mg, 0.14 mmol) was dissolved in DMF (5 mL), 1-(2-chloro-5-(9-(piperazin-1-ylmethyl) was added )-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (84 mg, 0.17 mmol), DIEA (55 mg, 0.42 mmol) and pyBOP (88 mg, 0.17 mmol), react at room temperature for 1 h, add water (50 mL) and stir for 5 minutes, extract with ethyl acetate (30 mL×3), wash the organic phase with saturated brine (50 mL), dry over anhydrous sodium sulfate, Filtered, concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to give 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino- 5-(trifluoromethyl)phenyl)ethyl)amino)-2,7-dimethylquinazolin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl) -3-Azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝970.4. LC-MS: (ESI, m/z): [M+H] + = 970.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.19(d,J＝8.0Hz,1H),8.08(s,1H),7.64(d,J＝8.2Hz,1H),7.55(d,J＝1.9Hz,1H),7.45–7.31(m,2H),6.87(d,J＝11.3Hz,2H),6.70(s,1H),5.67–5.45(m,3H),3.82-3.70(m,1H),3.67–3.42(m,8H),2.87–2.64(m,5H),2.43(s,3H),2.39-2.22(m,7H),2.18-2.09(m,2H),1.90-1.78(m,4H),1.73-1.24(m,14H),1.18-0.94(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51(s, 1H), 8.19(d, J=8.0Hz, 1H), 8.08(s, 1H), 7.64(d, J=8.2Hz, 1H) ,7.55(d,J＝1.9Hz,1H),7.45-7.31(m,2H),6.87(d,J＝11.3Hz,2H),6.70(s,1H),5.67-5.45(m,3H), 3.82-3.70(m, 1H), 3.67-3.42(m, 8H), 2.87-2.64(m, 5H), 2.43(s, 3H), 2.39-2.22(m, 7H), 2.18-2.09(m, 2H ),1.90-1.78(m,4H),1.73-1.24(m,14H),1.18-0.94(m,4H).
实施例73：1-(2-甲氧基-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 73: 1-(2-Methoxy-5-(9-(((4-((1R,4R)-4-(7-methoxy-2-methyl-4-((((R)) -1-(4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine -1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯的制备Step 1: (2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)-4-methoxybenzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexane)- Preparation of 7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-001001
Figure PCTCN2022088560-appb-001001
将3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酸五氟苯酯(118mg,0.27mmol)和(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸(300mg,0.34mmol)溶解在DMSO(6mL)中，然后加入DIEA(132mg,1.02mmol)。反应液在室温搅拌2h。反应用水(50mL)稀释，用EA(50mLx3)。合并有机相，用食盐水(50mL)洗涤，无水硫酸钠干燥，过滤，减压浓缩。粗品经柱层析(/MeOH(NH 3)/DCM 0％～20％)纯化得到(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯。 3-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoic acid pentafluorophenyl ester (118 mg, 0.27 mmol) and (2-(5-((R )-1-((6-((1R,4R)-4-(4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl )-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylic acid (300 mg, 0.34 mmol) was dissolved in DMSO ( 6 mL), then DIEA (132 mg, 1.02 mmol) was added. The reaction solution was stirred at room temperature for 2 h. The reaction was diluted with water (50 mL) with EA (50 mL x 3). The organic phases were combined, washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (/MeOH( NH3 )/DCM 0%-20%) to give (2-(5-((R)-1-((6-((1R,4R)-4-(4 -((3-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoyl)-3-azaspiro[5.5]undecane- 9-yl)methyl)piperazine-1-carbonyl)cyclohexane)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl ) (methyl) tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M/2+H] +＝563.5. LC-MS: (ESI, m/z): [M/2+H] + = 563.5.
步骤2：1-(2-甲氧基-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Methoxy-5-(9-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)- 1-(4-(2-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine- Preparation of 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-001002
Figure PCTCN2022088560-appb-001002
室温时，搅拌下向(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-甲氧基苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己烷)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基) 苄基)(甲基)羧酸叔丁酯(72mg,0.064mmol)的DCM(3mL)溶液中加TFA(1ml)，反应液在室温搅拌2h。反应液直接减压浓缩。粗品经prep-HPLC纯化得到1-(2-甲氧基-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。At room temperature, under stirring (2-(5-((R)-1-(((6-((1R,4R)-4-(4-((3-(3-(2,4-dioxo Tetrahydropyrimidin-1(2H)-yl)-4-methoxybenzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl Alkyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylate tert-butyl ester (72 mg, 0.064 mmol) TFA (1 ml) was added to the DCM (3 mL) solution, and the reaction solution was stirred at room temperature for 2 h. The reaction solution was directly concentrated under reduced pressure. The crude product was purified by prep-HPLC to give 1-(2-methoxy-5-(9-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(( (R)-1-(4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl )piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1024.4. LC-MS: (ESI, m/z): [M+H] + = 1024.4.
1H NMR(400MHz,CD 3OD)δ7.99(s,1H),7.46–7.36(m,3H),7.34–7.27(m,3H),7.22-7.12(m,3H),7.01(s,1H),6.10-6.02(m,1H),3.95-3.91(m,6H),3.75-3.45(m,12H),3.12-3.01(m,1H),2.80(t,J＝6.7Hz,2H),2.75–2.66(m,1H),2.52(s,3H),2.44(m,2H),2.38(m,2H),2.25–2.16(m,5H),2.00–1.84(m,4H),1.79(d,J＝7.0Hz,4H),1.71-1.54(m,9H),1.37-1.12(m,7H). 1 H NMR (400MHz, CD 3 OD) δ 7.99(s, 1H), 7.46-7.36(m, 3H), 7.34-7.27(m, 3H), 7.22-7.12(m, 3H), 7.01(s, 1H), 6.10-6.02(m, 1H), 3.95-3.91(m, 6H), 3.75-3.45(m, 12H), 3.12-3.01(m, 1H), 2.80(t, J=6.7Hz, 2H) ,2.75–2.66(m,1H),2.52(s,3H),2.44(m,2H),2.38(m,2H),2.25–2.16(m,5H),2.00–1.84(m,4H),1.79 (d, J=7.0Hz, 4H), 1.71-1.54 (m, 9H), 1.37-1.12 (m, 7H).
实施例74：1-(2-氟-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 74: 1-(2-Fluoro-5-(9-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-((((R)-1) -(4-(2-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1 -yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯的制备Step 1: (2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)-4-fluorobenzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-methyl Preparation of tert-butyl oxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylate
Figure PCTCN2022088560-appb-001003
将3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酸五氟苯酯(133mg,0.32mmol)和(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯(350mg,0.39mmol)溶解在DMSO(6mL)中，然后加入DIEA(132mg,1.02mmol)。反应液在室温搅拌2h。反应结束后，反应液用水(50mL)稀释，并用EA(50mLx3)萃取。合并有机相，用饱和食盐水(50mL)洗涤，无水硫酸钠干燥，过滤并减压浓缩。粗品经柱层析(MeOH(NH 3)/DCM,0％～20％)纯化得到(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯。
Figure PCTCN2022088560-appb-001003
3-(2,4-Dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoic acid pentafluorophenyl ester (133 mg, 0.32 mmol) and (2-(5-((R)- 1-((6-((1R,4R)-4-(4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)- 7-Methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylate tert-butyl ester (350 mg, 0.39 mmol) was dissolved in DMSO (6 mL), then DIEA (132 mg, 1.02 mmol) was added. The reaction solution was stirred at room temperature for 2 h. After the reaction, the reaction solution was diluted with water (50 mL) and extracted with EA (50 mL×3). The organic phases were combined, washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (MeOH( NH3 )/DCM, 0%-20%) to give (2-(5-((R)-1-((6-((1R,4R)-4-(4 -((3-(3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)-4-fluorobenzoyl)-3-azaspiro[5.5]undecan-9- (methyl)methyl)piperazine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl) base) tert-butyl carboxylate.
LC-MS:(ESI,m/z):[M/2+H] +＝556.9. LC-MS: (ESI, m/z): [M/2+H] + =556.9.
步骤2：1-(2-氟-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Fluoro-5-(9-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R)-1- (4-(2-((Methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperazine-1- Preparation of (yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-001004
Figure PCTCN2022088560-appb-001004
室温下，向(2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-二氧代四氢嘧啶-1(2H)-基)-4-氟苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)噻吩-3-基)苄基)(甲基)羧酸叔丁酯(100mg,0.09mmol)的DCM(3mL)溶液中加入TFA(1ml)。反应液在室温搅拌2h。反应液直接浓缩。粗品经prep-HPLC纯化得到1-(2-氟-5-(9-((4-((1R,4R)-4-(7-甲氧基-2-甲基-4-(((R)-1-(4-(2-((甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)喹唑啉-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。At room temperature, to (2-(5-((R)-1-((6-((1R,4R)-4-(4-((3-(3-(2,4-dioxotetrahydro Pyrimidine-1(2H)-yl)-4-fluorobenzoyl)-3-azaspiro[5.5]undecan-9-yl)methyl)piperazine-1-carbonyl)cyclohexyl)-7- Methoxy-2-methylquinazolin-4-yl)amino)ethyl)thiophen-3-yl)benzyl)(methyl)carboxylate (100 mg, 0.09 mmol) in DCM (3 mL) To the solution was added TFA (1 ml). The reaction solution was stirred at room temperature for 2 h. The reaction solution was directly concentrated. The crude product was purified by prep-HPLC to give 1-(2-fluoro-5-(9-((4-((1R,4R)-4-(7-methoxy-2-methyl-4-(((R )-1-(4-(2-((methylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)quinazolin-6-yl)cyclohexane-1-carbonyl)piperidine oxazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1012.3. LC-MS: (ESI, m/z): [M+H] + = 1012.3.
1H NMR(400MHz,CD 3OD)δ7.99(s,1H),7.52(dd,J＝7.1,1.9Hz,1H),7.46-7.39(m,2H),7.36-7.27(m, 4H),7.21-7.17(m,1H),7.15-7.11(m,1H),7.01(s,1H),6.08-6.03(m,1H),3.95(s,3H),3.83(t,J＝6.7Hz,2H),3.77–3.55(m,8H),3.50-3.37(m,2H),3.10-3.00(m,1H),2.83(t,J＝6.7Hz,2H),2.76-2.65(m,1H),2.52(s,3H),2.44(b,2H),2.38(b,2H),2.25-2.16(m,5H),2.00-1.83(m,4H),1.82-1.75(m,4H),1.69–1.46(m,9H),1.36-1.06(m,7H). 1 H NMR (400 MHz, CD 3 OD) δ 7.99 (s, 1H), 7.52 (dd, J=7.1, 1.9 Hz, 1H), 7.46-7.39 (m, 2H), 7.36-7.27 (m, 4H) ,7.21-7.17(m,1H),7.15-7.11(m,1H),7.01(s,1H),6.08-6.03(m,1H),3.95(s,3H),3.83(t,J=6.7Hz ,2H),3.77-3.55(m,8H),3.50-3.37(m,2H),3.10-3.00(m,1H),2.83(t,J＝6.7Hz,2H),2.76-2.65(m,1H) ), 2.52(s, 3H), 2.44(b, 2H), 2.38(b, 2H), 2.25-2.16(m, 5H), 2.00-1.83(m, 4H), 1.82-1.75(m, 4H), 1.69-1.46(m,9H),1.36-1.06(m,7H).
实施例75：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮 Example 75: 1-(5-(4-(((1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)methyl-d 2 ) Piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(羟基甲基-d 2)哌啶-1-羧酸叔丁酯的制备 Step 1: Preparation of tert-butyl 4-(hydroxymethyl- d2 )piperidine-1-carboxylate
Figure PCTCN2022088560-appb-001005
Figure PCTCN2022088560-appb-001005
1-(叔丁基)4-乙基哌啶-1,4-二羧酸盐(500mg,1.93mmol)溶解于乙醇中(20mL)，0℃下加入NaBD 4(325mg,7.75mmol)并搅拌2小时。反应液中加入水(30mL)，用乙酸乙酯(30mLx3)萃取。有机相用饱和食盐水(100mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(乙酸乙酯:石油醚＝1:1)纯化得到4-(羟基甲基-d 2)哌啶-1-羧酸叔丁酯。 1-(tert-butyl)4-ethylpiperidine-1,4-dicarboxylate (500 mg, 1.93 mmol) was dissolved in ethanol (20 mL), NaBD 4 (325 mg, 7.75 mmol) was added at 0°C and stirred 2 hours. Water (30 mL) was added to the reaction solution, followed by extraction with ethyl acetate (30 mL×3). The organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified using column chromatography (ethyl acetate:petroleum ether=1:1) to obtain tert-butyl 4-(hydroxymethyl-d 2 )piperidine-1-carboxylate.
1H NMR(400MHz,DMSO-d 6)δ4.42(s,1H),3.93(d,J＝11.9Hz,2H),2.67(s,2H),1.62(d,J＝12.9Hz,2H),1.55–1.44(m,1H),1.39(s,9H),0.96(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 4.42(s, 1H), 3.93(d, J=11.9Hz, 2H), 2.67(s, 2H), 1.62(d, J=12.9Hz, 2H) ,1.55–1.44(m,1H),1.39(s,9H),0.96(m,2H).
步骤2：4-((吡啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯的制备 Step 2: Preparation of tert-butyl 4-((pyridin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate
Figure PCTCN2022088560-appb-001006
Figure PCTCN2022088560-appb-001006
4-(羟基甲基-d 2)哌啶-1-羧酸叔丁酯(250mg,1.14mmol)溶于无水四氢呋喃(10mL)中，氮气氛围下降温至0℃并加入NaH(364mg,9.12mmol)，搅拌3小时后，加入4-(溴甲基)吡啶氢溴酸盐(576mg,2.28mmol)，室温搅拌过夜。反应液中加入水(20mL)，用乙酸乙酯(20mLx3)萃取。有机相用饱和食盐水(60mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩。粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-((吡啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯。 4-(Hydroxymethyl-d 2 )piperidine-1-carboxylate tert-butyl ester (250 mg, 1.14 mmol) was dissolved in dry tetrahydrofuran (10 mL), warmed to 0 °C under nitrogen atmosphere and NaH (364 mg, 9.12 mmol) was added. mmol), and after stirring for 3 hours, 4-(bromomethyl)pyridine hydrobromide (576 mg, 2.28 mmol) was added, and the mixture was stirred at room temperature overnight. Water (20 mL) was added to the reaction solution, followed by extraction with ethyl acetate (20 mL×3). The organic phase was washed with saturated brine (60 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified using column chromatography (methanol:dichloromethane=1:9) to obtain tert-butyl 4-((pyridin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝309.1 LC-MS: (ESI, m/z): [M+H] + = 309.1
1H NMR(400MHz,DMSO-d 6)δ8.53(dd,J＝4.5,1.5Hz,2H),7.31(d,J＝5.8Hz,2H),4.51(s,2H),3.94(d,J＝12.0Hz,2H),2.70(s,2H),1.76(m,1H),1.67(d,J＝12.9Hz,2H),1.39(s,9H),1.06(m,2H). 1 H NMR (400MHz, DMSO-d 6 ) δ 8.53 (dd, J=4.5, 1.5 Hz, 2H), 7.31 (d, J=5.8 Hz, 2H), 4.51 (s, 2H), 3.94 (d, J=12.0Hz, 2H), 2.70(s, 2H), 1.76(m, 1H), 1.67(d, J=12.9Hz, 2H), 1.39(s, 9H), 1.06(m, 2H).
步骤3：4-((哌啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯的制备 Step 3: Preparation of tert-butyl 4-((piperidin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate
Figure PCTCN2022088560-appb-001007
Figure PCTCN2022088560-appb-001007
将4-((吡啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯(180mg,0.58mmol)溶于异丙醇(10mL)和水(10mL)中，加入Pd/C(60mg,0.058mmol)，在氢气氛围下升温至70℃并搅拌过夜。反应液冷却至室温，过滤，滤液减压浓缩得到4-((哌啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯，粗品无需纯化直接用于下一步反应。 4-((Pyridin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate tert-butyl ester (180 mg, 0.58 mmol) was dissolved in isopropanol (10 mL) and water (10 mL) , added Pd/C (60 mg, 0.058 mmol), heated to 70 °C under a hydrogen atmosphere and stirred overnight. The reaction solution was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain tert-butyl 4-((piperidin-4-ylmethoxy)methyl-d 2 )piperidine-1-carboxylate. The crude product was used directly without purification. next reaction.
LC-MS:(ESI,m/z):[M+H] +＝315.2. LC-MS: (ESI, m/z): [M+H] + = 315.2.
步骤4：4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯的制备 Step 4: 4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl) )phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)methyl- d 2 ) Preparation of tert-butyl piperidine-1-carboxylate
Figure PCTCN2022088560-appb-001008
Figure PCTCN2022088560-appb-001008
将4-((哌啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯(130mg,0.41mmol)溶解于DMF(10mL)中，加入(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.25mmol)，HATU(123mg,0.32mmol)和DIEA(96mg,0.74mmol)，室温下搅拌1小时。反应液用水(100mL)稀释，用乙酸乙酯(30mLx3)萃取，有机相用饱和食盐水(50mL)洗涤，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯。 4-((Piperidin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate tert-butyl ester (130 mg, 0.41 mmol) was dissolved in DMF (10 mL), (1R,4R) was added )-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.25 mmol), HATU (123 mg, 0.32 mmol) and DIEA (96 mg, 0.74 mmol) and stirred at room temperature for 1 hour. The reaction solution was diluted with water (100 mL), extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and the crude product was subjected to column chromatography (methanol: two Chloromethane=1:9) purification to give 4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5 -(Trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methan Oxy)methyl- d2 )piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝899.5. LC-MS: (ESI, m/z): [M+H] + = 899.5.
步骤5：((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-基)甲酮的制备 Step 5: ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy - Preparation of 2-methylquinazolin-6-yl)cyclohexyl)(4-((piperidin-4-ylmethoxy-d 2 )methyl)piperidin-1-yl)methanone
Figure PCTCN2022088560-appb-001009
Figure PCTCN2022088560-appb-001009
将4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯(200mg,0.22mmol)溶解于DCM(5mL)中，加入TFA(2mL)，室温下搅拌2小时。反应液直接减压浓缩得到((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-基)甲酮。 4-(((1-((1R,4R)-4-(4-(((R)-1-(3-((tert-butoxycarbonyl)amino)-5-(trifluoromethyl)benzene (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)methyl-d 2 ) piperidine-1-carboxylate tert-butyl ester (200 mg, 0.22 mmol) was dissolved in DCM (5 mL), TFA (2 mL) was added, and the mixture was stirred at room temperature for 2 hours. The reaction solution was directly concentrated under reduced pressure to obtain ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7 -Methoxy-2-methylquinazolin-6-yl)cyclohexyl)(4-((piperidin-4-ylmethoxy- d2 )methyl)piperidin-1-yl)methanone .
LC-MS:(ESI,m/z):[M+H] +＝699.4 LC-MS: (ESI, m/z): [M+H] + = 699.4
步骤6：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 6: 1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) (yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy)methyl-d 2 ) piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione preparation
Figure PCTCN2022088560-appb-001010
Figure PCTCN2022088560-appb-001010
将((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己基)(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-基)甲酮(粗产品,200mg,0.22mmol)溶于DMSO(10mL)中，然后加4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(95mg,0.22mmol)和DIEA(86mg,0.66mmol)，室温下搅拌2小时。向反应液中加入水(100mL)，用二氯甲烷(30mLx3)萃取，有机相减压浓缩得到粗品。粗品经pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 ((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2 -Methylquinazolin-6-yl)cyclohexyl)(4-((piperidin-4-ylmethoxy-d 2 )methyl)piperidin-1-yl)methanone (crude product, 200 mg, 0.22 mmol) was dissolved in DMSO (10 mL), followed by the addition of pentafluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (95 mg, 0.22 mmol) and DIEA (86 mg, 0.66 mmol) and stirred at room temperature for 2 hours. Water (100 mL) was added to the reaction solution, extracted with dichloromethane (30 mL×3), and the organic phase was concentrated under reduced pressure to obtain a crude product. The crude product was purified by pre-HPLC ( CH3CN /0.08% aqueous NH4HCO3 , 5 %~95%) to give 1-(5-(4-(((1-((1R,4R)-4-(4 -(((R)-1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cycle Hexane-1-carbonyl)piperidin-4-yl)methoxy)methyl- d2 )piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H) - Diketones.
LC-MS:(ESI,m/z):[M+H] +＝949.4. LC-MS: (ESI, m/z): [M+H] + = 949.4.
1H NMR(400MHz,DMSO-d 6)δδ10.50(s,1H),8.15–8.02(m,2H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.8Hz,1H),7.38(dd,J＝8.2,1.9Hz,1H),6.99(s,1H),6.87(s,1H),6.85(s,1H),6.70(s,1H),5.63–5.48(m,3H),4.51-4.36(m,2H),3.99–3.86(m,4H),3.78-3.71(m,1H),3.65-3.53(m,2H),3.23(d,J＝6.1Hz,2H),3.09-2.90(m,3H),2.81-2.62(m,4H),2.35(s,3H),1.91–1.52(m,18H),1.18-0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δδ10.50(s,1H),8.15-8.02(m,2H),7.63(d,J=8.2Hz,1H),7.54(d,J=1.8Hz, 1H), 7.38(dd, J=8.2, 1.9Hz, 1H), 6.99(s, 1H), 6.87(s, 1H), 6.85(s, 1H), 6.70(s, 1H), 5.63–5.48(m ,3H),4.51-4.36(m,2H),3.99-3.86(m,4H),3.78-3.71(m,1H),3.65-3.53(m,2H),3.23(d,J=6.1Hz,2H ), 3.09-2.90(m, 3H), 2.81-2.62(m, 4H), 2.35(s, 3H), 1.91-1.52(m, 18H), 1.18-0.92(m, 4H).
实施例76：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基-d 2)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮 Example 76: 1-(5-(4-(((1-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)) Phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy- d2 )methyl yl)piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯的制备 Step 1: 4-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy ) Preparation of methyl-d 2 ) piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-001011
Figure PCTCN2022088560-appb-001011
将4-((哌啶-4-基甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯(180mg,0.57mmol)用二甲亚砜(5mL)溶解，然后加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(247mg,0.57mmol)和N,N-二异丙基乙胺(220mg,1.71mmol)，反应液室温下搅拌2小时，加水(50mL)稀释，用二氯甲烷(30mLx3)萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯。 Dissolve tert-butyl 4-((piperidin-4-ylmethoxy)methyl- d2 )piperidine-1-carboxylate (180 mg, 0.57 mmol) in dimethylsulfoxide (5 mL), then add 4 - Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)pentafluorophenyl benzoate (247mg, 0.57mmol) and N,N-diisopropylethylamine (220mg, 1.71 mmol), the reaction solution was stirred at room temperature for 2 hours, diluted with water (50 mL), extracted with dichloromethane (30 mL×3), the organic phase was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (methanol:dichloromethane=1:9) to give 4-(((1-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) ) benzoyl)piperidin-4-yl)methoxy)methyl- d2 )piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝565.2. LC-MS: (ESI, m/z): [M+H] + = 565.2.
步骤2：1-(2-氯-5-(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 2: 1-(2-Chloro-5-(4-((piperidin-4-ylmethoxy- d2 )methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4 Preparation of (1H,3H)-dione
Figure PCTCN2022088560-appb-001012
Figure PCTCN2022088560-appb-001012
将4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羧酸叔丁酯(220mg,0.39mmol)用二氯甲烷(5mL)溶解，然后加入三氟乙酸(2mL)，反应液室温搅拌2小时，直接减压浓缩得到1-(2-氯-5-(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮，无需纯化直接用于下一步反应。 4-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)methane tert-butyl-d 2 )piperidine-1-carboxylate (220 mg, 0.39 mmol) was dissolved in dichloromethane (5 mL), then trifluoroacetic acid (2 mL) was added, the reaction solution was stirred at room temperature for 2 hours, and directly concentrated under reduced pressure 1-(2-Chloro-5-(4-((piperidin-4-ylmethoxy- d2 )methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H ,3H)-dione, which was used in the next step without purification.
LC-MS:(ESI,m/z):[M+H] +＝465.3. LC-MS: (ESI, m/z): [M+H] + = 465.3.
步骤3：(3-((R)-1-((6-((1R,4R)-4-(4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯的制备 Step 3: (3-((R)-1-((6-((1R,4R)-4-(4-((((1-(4-chloro-3-(2,4-dioxotetra) Hydropyrimidin-1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)methyl- d2 )piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2- Preparation of methylquinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-001013
Figure PCTCN2022088560-appb-001013
将1-(2-氯-5-(4-((哌啶-4-基甲氧基-d 2)甲基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(220mg,0.39mmol)用DMF(10mL)溶解，然后分别加入(1R,4R)-4-(4-(((R)-1-(3-((叔丁氧羰基)氨基)-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(150mg,0.24mmol)，HATU(118mg,0.31mmol)和N,N-二异丙基乙胺(93mg,0.72mmol)，室温下搅拌2小时，加水(100mL)，用乙酸乙酯(30mLx3)萃取，饱和食盐水(100mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(甲醇:二氯甲烷＝1:9)纯化得到(3-((R)-1-((6-((1R,4R)-4-(4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯。 1-(2-Chloro-5-(4-((piperidin-4-ylmethoxy-d 2 )methyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H ,3H)-dione (220 mg, 0.39 mmol) was dissolved in DMF (10 mL), then (1R,4R)-4-(4-((((R)-1-(3-((tert-butoxycarbonyl) was then added separately. ) amino)-5-(trifluoromethyl)phenyl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (150 mg, 0.24 mmol), HATU (118 mg, 0.31 mmol) and N,N-diisopropylethylamine (93 mg, 0.72 mmol), stirred at room temperature for 2 hours, added water (100 mL), extracted with ethyl acetate (30 mL×3), saturated The organic phase was washed with brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (methanol:dichloromethane=1:9) to obtain (3-((R)-1- ((6-((1R,4R)-4-(4-((((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl) )piperidin-4-yl)methoxy)methyl-d 2 )piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methylquinazolin-4-yl)amino)ethyl yl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝1049.3. LC-MS: (ESI, m/z): [M+H] + = 1049.3.
步骤4：1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基-d 2)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备 Step 4: 1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)benzene) yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy- d2 )methyl ) piperidine-1-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione preparation
Figure PCTCN2022088560-appb-001014
Figure PCTCN2022088560-appb-001014
将(3-((R)-1-((6-((1R,4R)-4-(4-(((1-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)哌啶-4-基)甲氧基)甲基-d 2)哌啶-1-羰基)环己基)-7-甲氧基-2-甲基喹唑啉-4-基)氨基)乙基)-5-(三氟甲基)苯基)羧酸叔丁酯(200mg,0.19mmol)用二氯甲烷(5mL)溶解，加入三氟乙酸(2mL)，室温搅拌2小时后，反应液减压浓缩，所得粗产物用10％甲醇/二氯甲烷混合溶液(20mL)溶解，然后加入5％碳酸氢钠水溶液(20mL)并搅拌1小时，静置分离，有机相经无水硫酸钠干燥，过滤，减压浓缩得到粗品，粗品经pre-HPLC(CH 3CN/0.08％NH 4HCO 3水溶液,5％～95％)纯化得到1-(5-(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)甲氧基-d 2)甲基)哌啶-1-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。 (3-((R)-1-((6-((1R,4R)-4-(4-(((1-(4-Chloro-3-(2,4-dioxotetrahydropyrimidine) -1(2H)-yl)benzoyl)piperidin-4-yl)methoxy)methyl- d2 )piperidine-1-carbonyl)cyclohexyl)-7-methoxy-2-methyl Quinazolin-4-yl)amino)ethyl)-5-(trifluoromethyl)phenyl)carboxylate tert-butyl ester (200 mg, 0.19 mmol) was dissolved in dichloromethane (5 mL), trifluoroacetic acid ( 2 mL), after stirring at room temperature for 2 hours, the reaction solution was concentrated under reduced pressure, and the obtained crude product was dissolved in a 10% methanol/dichloromethane mixed solution (20 mL), and then 5% aqueous sodium bicarbonate solution (20 mL) was added and stirred for 1 hour, and the mixture was stirred for 1 hour. It was separated, the organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain the crude product. The crude product was purified by pre-HPLC (CH 3 CN/0.08% aqueous NH 4 HCO 3 solution, 5%-95%) to obtain 1-(5 -(4-(((1-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -7-Methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)methoxy- d2 )methyl)piperidine-1-carbonyl )-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝949.2. LC-MS: (ESI, m/z): [M+H] + = 949.2.
1H NMR(400MHz,DMSO-d 6)δ10.49(s,1H),8.13(d,J＝7.7Hz,1H),8.06(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝2.0Hz,1H),7.37(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.86(d,J＝10.1Hz,2H),6.70(s,1H),5.57(dd,J＝17.7,10.2Hz,3H),4.42(d,J＝12.0Hz,2H),3.92(m,4H),3.81–3.51(m,3H),3.24(d,J＝6.2Hz,2H),3.09–2.88(m,3H),2.78–2.60(m,4H),2.36(s,3H),1.90–1.52(m,18H),1.19–0.92(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.49(s, 1H), 8.13(d, J=7.7Hz, 1H), 8.06(s, 1H), 7.63(d, J=8.2Hz, 1H) ,7.54(d,J＝2.0Hz,1H),7.37(dd,J＝8.2,2.0Hz,1H),6.99(s,1H),6.86(d,J＝10.1Hz,2H),6.70(s, 1H), 5.57(dd, J＝17.7, 10.2Hz, 3H), 4.42(d, J＝12.0Hz, 2H), 3.92(m, 4H), 3.81–3.51(m, 3H), 3.24(d, J = 6.2Hz, 2H), 3.09–2.88 (m, 3H), 2.78–2.60 (m, 4H), 2.36 (s, 3H), 1.90–1.52 (m, 18H), 1.19–0.92 (m, 4H).
实施例77：(R)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)-N-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)乙酰胺Example 77: (R)-2-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazoline- 6-yl)piperidin-1-yl)-N-(2-(3-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl) -3-Azaspiro[5.5]undecan-9-yl)ethyl)acetamide
步骤1：6-溴-2-甲基喹唑啉-4-醇的制备Step 1: Preparation of 6-bromo-2-methylquinazolin-4-ol
Figure PCTCN2022088560-appb-001015
Figure PCTCN2022088560-appb-001015
将2-氨基-5-溴苯甲酰胺(4.0g,14.55mmol)加入到原乙酸三甲酯(17.46g,145.5mmol)的甲醇(100mL)溶液中，在闷罐中120℃搅拌过夜，冷却后减压浓缩，得到粗产品6-溴-2-甲基喹唑啉-4-醇，无需纯化直接用于下步反应。2-Amino-5-bromobenzamide (4.0 g, 14.55 mmol) was added to a solution of trimethyl orthoacetate (17.46 g, 145.5 mmol) in methanol (100 mL), stirred at 120 °C overnight in a stuffy tank, cooled After concentrating under reduced pressure, the crude product 6-bromo-2-methylquinazolin-4-ol was obtained, which was directly used in the next reaction without purification.
LC-MS:(ESI,m/z):[M+H] +＝238.9. LC-MS: (ESI, m/z): [M+H] + = 238.9.
步骤2：4-(4-羟基-2-甲基喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯的制备Step 2: Preparation of 4-(4-hydroxy-2-methylquinazolin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-001016
Figure PCTCN2022088560-appb-001016
将6-溴-2-甲基喹唑啉-4-醇(5.00g,16.67mmol)用DMF/H 2O(200mL/20ml)溶解，然后分别加入碳酸钾(5.80g,42.03mmol)，Pd(dppf)Cl 2(1.54g,2.10mmol)和4-(4,4,5,5-四甲基-1,3,2-二氧硼戊烷-2-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯(7.79g,25.21mmol)，反应液在氮气保护下110℃搅拌过夜，加水(500mL)稀释，用乙酸乙酯(200mL×3)萃取，有机相用饱和食盐水洗(200mL)，无水硫酸钠干燥，过滤，减压浓缩，粗品使用柱层析(PE:EA＝1:2)纯化得到4-(4-羟基-2-甲基喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯。 6-Bromo-2-methylquinazolin-4-ol (5.00 g, 16.67 mmol) was dissolved in DMF/H 2 O (200 mL/20 ml), then potassium carbonate (5.80 g, 42.03 mmol), Pd (dppf)Cl 2 (1.54 g, 2.10 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboropentan-2-yl)-3,6-di Hydropyridine-1(2H)-carboxylate tert-butyl ester (7.79g, 25.21mmol), the reaction solution was stirred at 110°C overnight under nitrogen protection, diluted with water (500mL), extracted with ethyl acetate (200mL×3), organic The phase was washed with saturated brine (200 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography (PE:EA=1:2) to obtain 4-(4-hydroxy-2-methylquinazole). olin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylic acid tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝342.1. LC-MS: (ESI, m/z): [M+H] + = 342.1.
步骤3：4-(4-羟基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯的制备Step 3: Preparation of tert-butyl 4-(4-hydroxy-2-methylquinazolin-6-yl)piperidine-1-carboxylate
Figure PCTCN2022088560-appb-001017
Figure PCTCN2022088560-appb-001017
将4-(4-羟基-2-甲基喹唑啉-6-基)-3,6-二氢吡啶-1(2H)-羧酸叔丁酯(2.5g,14.55mmol)加入到Pd(OH) 2(800mg,20％)的甲醇(100mL)溶液中，在H 2氛围下高压釜中70℃搅拌过夜(10atm)，冷却后过滤，减压浓缩，得到粗产品4-(4-羟基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯。 4-(4-Hydroxy-2-methylquinazolin-6-yl)-3,6-dihydropyridine-1(2H)-carboxylate tert-butyl ester (2.5 g, 14.55 mmol) was added to Pd ( OH) 2 (800 mg, 20%) in methanol (100 mL) solution, stirred overnight (10 atm) at 70 °C in an autoclave under H 2 atmosphere, cooled, filtered, and concentrated under reduced pressure to obtain the crude product 4-(4-hydroxyl - 2-Methylquinazolin-6-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝344.1. LC-MS: (ESI, m/z): [M+H] + = 344.1.
步骤4：(R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯的制备Step 4: (R)-4-(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl ) Preparation of piperidine-1-carboxylate tert-butyl ester
Figure PCTCN2022088560-appb-001018
Figure PCTCN2022088560-appb-001018
将BOP(3.30g,7.47mmol)和DBU(1.90g,12.5mmol)和(R)-1-(3-硝基-5-(三氟甲基)苯基)乙烷-1-胺(1.53g,6.54mmol)分别加入到4-(4-羟基-2-甲基喹唑啉-6-基)哌啶-1-羧酸叔丁酯(1.73g,5.03mmol)的DMF(100mL)溶液中，反应液70℃搅拌过夜，用水(300mL)稀释，乙酸乙酯(100mL)萃取，饱和食盐水(150mL)洗涤有机相，经无水硫酸钠干燥，过滤，减压浓缩，粗品使用反相柱层析(H 2O:ACN＝1:2)纯化得到(R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯。 BOP (3.30 g, 7.47 mmol) and DBU (1.90 g, 12.5 mmol) and (R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethane-1-amine (1.53 g, 6.54 mmol) were added to a solution of 4-(4-hydroxy-2-methylquinazolin-6-yl) piperidine-1-carboxylate tert-butyl ester (1.73 g, 5.03 mmol) in DMF (100 mL), respectively The reaction solution was stirred at 70°C overnight, diluted with water (300 mL), extracted with ethyl acetate (100 mL), washed with saturated brine (150 mL), and the organic phase was washed with saturated brine (150 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. Purification by column chromatography (H 2 O:ACN=1:2) gave (R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl) )ethyl)amino)quinazolin-6-yl)piperidine-1-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝560.4. LC-MS: (ESI, m/z): [M+H] + = 560.4.
步骤5：(R)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺的制备Step 5: (R)-2-Methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidin-4-yl)quinazole Preparation of olin-4-amines
Figure PCTCN2022088560-appb-001019
Figure PCTCN2022088560-appb-001019
将(R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-羧酸叔丁酯(300mg,0.537mmol)加入到TFA(2mL)的二氯甲烷(20mL)中，常温搅拌1小时，减压浓缩，得到粗产品(R)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺。(R)-4-(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)piperidine Pyridin-1-carboxylate tert-butyl ester (300 mg, 0.537 mmol) was added to TFA (2 mL) in dichloromethane (20 mL), stirred at room temperature for 1 hour, and concentrated under reduced pressure to obtain the crude product (R)-2-methyl -N-(1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidin-4-yl)quinazolin-4-amine.
LC-MS:(ESI,m/z):[M+H] +＝460.4. LC-MS: (ESI, m/z): [M+H] + = 460.4.
步骤6：(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸叔丁酯的制备Step 6: (R)-2-(4-(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline- Preparation of 6-yl)piperidin-1-yl)acetate tert-butyl ester
Figure PCTCN2022088560-appb-001020
Figure PCTCN2022088560-appb-001020
将(R)-2-甲基-N-(1-(3-硝基-5-(三氟甲基)苯基)乙基)-6-(哌啶-4-基)喹唑啉-4-胺(250mg,0.543mmol)和碳酸钾(300mg,2.17mmol)加入到2-溴乙酸叔丁酯(138mg,0.708mmol)的THF(20mL)溶液中并在70℃搅拌过夜，反应液用水稀释(50ml)，用乙酸乙酯(50mL×3)萃取，用无水硫酸钠干燥，过滤，减压浓缩，粗品经柱层析(PE:EA＝5:1)纯化得到(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸叔丁酯。(R)-2-Methyl-N-(1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)-6-(piperidin-4-yl)quinazoline- 4-amine (250 mg, 0.543 mmol) and potassium carbonate (300 mg, 2.17 mmol) were added to a solution of tert-butyl 2-bromoacetate (138 mg, 0.708 mmol) in THF (20 mL) and stirred at 70 °C overnight, the reaction solution was water Diluted (50ml), extracted with ethyl acetate (50mL×3), dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, the crude product was purified by column chromatography (PE:EA=5:1) to obtain (R)-2 -(4-(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)piperidine-1 - base) tert-butyl acetate.
LC-MS:(ESI,m/z):[M+H] +＝574.3. LC-MS: (ESI, m/z): [M+H] + = 574.3.
步骤7：(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸的制 备Step 7: (R)-2-(4-(2-Methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline- Preparation of 6-yl)piperidin-1-yl)acetic acid
Figure PCTCN2022088560-appb-001021
Figure PCTCN2022088560-appb-001021
将(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸叔丁酯(300mg,0.524mmol)加入到HCl/1,4-二氧六环(4M,20mL)中，常温搅拌过夜，反应液直接减压浓缩，得到粗品(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸。(R)-2-(4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline-6- yl)piperidin-1-yl)acetic acid tert-butyl ester (300 mg, 0.524 mmol) was added to HCl/1,4-dioxane (4M, 20 mL), stirred at room temperature overnight, and the reaction solution was directly concentrated under reduced pressure to obtain Crude (R)-2-(4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline-6- yl)piperidin-1-yl)acetic acid.
LC-MS:(ESI,m/z):[M+H] +＝518.1. LC-MS: (ESI, m/z): [M+H] + = 518.1.
步骤8：(R)-9-(2-(2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 8: (R)-9-(2-(2-(4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl) Preparation of amino)quinazolin-6-yl)piperidin-1-yl)acetamide)ethyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester
Figure PCTCN2022088560-appb-001022
Figure PCTCN2022088560-appb-001022
将(R)-2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酸(167mg,0.323mmol)，HATU(154mg,0.405mmol)和DIEA(105mg,0.814mmol)加入到9-(2-氨乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(80mg,0.27mmol)的DMF(20mL)溶液中，反应液室温搅拌过夜，用水稀释(50mL)，用乙酸乙酯(50mL×3)萃取，粗品使用反相柱层析(ACN:H 2O＝1:3)纯化得到(R)-9-(2-(2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。 (R)-2-(4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazoline-6- [ 5.5] In a solution of tert-butyl undecane-3-carboxylate (80 mg, 0.27 mmol) in DMF (20 mL), the reaction solution was stirred at room temperature overnight, diluted with water (50 mL), extracted with ethyl acetate (50 mL×3), The crude product was purified by reverse phase column chromatography (ACN: H2O =1:3) to give (R)-9-(2-(2-(4-(2-methyl-4-((1-(3- Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)quinazolin-6-yl)piperidin-1-yl)acetamido)ethyl)-3-azaspiro[5.5]ten tert-Butyl monoalkane-3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝796.4. LC-MS: (ESI, m/z): [M+H] + = 796.4.
步骤9：(R)-9-(2-(2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯的制备Step 9: (R)-9-(2-(2-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methyl Preparation of tert-butyl quinazolin-6-yl)piperidin-1-yl)acetamide)ethyl)-3-azaspiro[5.5]undecan-3-carboxylate
Figure PCTCN2022088560-appb-001023
Figure PCTCN2022088560-appb-001023
将(R)-9-(2-(2-(4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(70mg,0.088mmol)用乙醇(10mL)溶解，然后分别加入Raney-Ni(0.3mL,水悬浮物)，水合肼一水合物(0.2mL)，反应液室温搅拌1小时,过滤，减压浓缩，得到粗品(R)-9-(2-(2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯。(R)-9-(2-(2-(4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino) Quinazolin-6-yl)piperidin-1-yl)acetamide)ethyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester (70 mg, 0.088 mmol) was treated with ethanol ( 10mL) was dissolved, then Raney-Ni (0.3mL, water suspension), hydrazine hydrate monohydrate (0.2mL) were added, the reaction solution was stirred at room temperature for 1 hour, filtered, and concentrated under reduced pressure to obtain crude product (R)-9- (2-(2-(4-(4-((1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazolin-6-yl) Piperidin-1-yl)acetamide)ethyl)-3-azaspiro[5.5]undecan-3-carboxylate tert-butyl ester.
LC-MS:(ESI,m/z):[M+H] +＝766.6. LC-MS: (ESI, m/z): [M+H] + = 766.6.
步骤10：(R)-N-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺的制备Step 10: (R)-N-(2-(3-Azaspiro[5.5]undecan-9-yl)ethyl)-2-(4-(4-((1-(3-amino- Preparation of 5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazolin-6-yl)piperidin-1-yl)acetamide
Figure PCTCN2022088560-appb-001024
Figure PCTCN2022088560-appb-001024
将(R)-9-(2-(2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺)乙基)-3-氮杂螺[5.5]十一烷-3-羧酸叔丁酯(65mg,0.085mmol)用DCM(10mL)溶解，加入TFA(1mL)，反应 液常温搅拌1小时，直接减压浓缩，得到粗产品(R)-N-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺。(R)-9-(2-(2-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinoline oxazolin-6-yl)piperidin-1-yl)acetamide)ethyl)-3-azaspiro[5.5]undecan-3-carboxylic acid tert-butyl ester (65 mg, 0.085 mmol) was dissolved in DCM (10 mL) ) was dissolved, TFA (1 mL) was added, the reaction solution was stirred at room temperature for 1 hour, and directly concentrated under reduced pressure to obtain the crude product (R)-N-(2-(3-azaspiro[5.5]undecan-9-yl) Ethyl)-2-(4-(4-((1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazolin-6-yl) piperidin-1-yl)acetamide.
LC-MS:(ESI,m/z):[M+H] +＝666.4. LC-MS: (ESI, m/z): [M+H] + = 666.4.
步骤11：(R)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)-N-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)乙酰胺的制备Step 11: (R)-2-(4-(4-((1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazoline-6 -yl)piperidin-1-yl)-N-(2-(3-(4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)- Preparation of 3-azaspiro[5.5]undecan-9-yl)ethyl)acetamide
Figure PCTCN2022088560-appb-001025
Figure PCTCN2022088560-appb-001025
将(R)-N-(2-(3-氮杂螺[5.5]十一烷-9-基)乙基)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)乙酰胺(50mg,0.075mmol)用DMSO(10mL)溶解，然后分别加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(40mg,0.092mmol)和DIEA(30mg,0.232mmol)，反应液室温搅拌过夜，用水稀释(20mL)，二氯甲烷萃取(30mL×3)，有机相减压浓缩，粗品使用反相制备纯化得到(R)-2-(4-(4-((1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基喹唑啉-6-基)哌啶-1-基)-N-(2-(3-(4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酰)-3-氮杂螺[5.5]十一烷-9-基)乙基)乙酰胺。(R)-N-(2-(3-azaspiro[5.5]undecan-9-yl)ethyl)-2-(4-(4-((1-(3-amino-5- (Trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazolin-6-yl)piperidin-1-yl)acetamide (50 mg, 0.075 mmol) was dissolved in DMSO (10 mL), then 4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl) benzoic acid pentafluorophenyl ester (40mg, 0.092mmol) and DIEA (30mg, 0.232mmol) were added respectively, the reaction solution Stir overnight at room temperature, dilute with water (20 mL), extract with dichloromethane (30 mL×3), concentrate the organic phase under reduced pressure, and purify the crude product using reverse-phase preparation to obtain (R)-2-(4-(4-((1-( 3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylquinazolin-6-yl)piperidin-1-yl)-N-(2-(3-( 4-Chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoyl)-3-azaspiro[5.5]undecan-9-yl)ethyl)ethyl amide.
LC-MS:(ESI,m/z):[M+H] +＝916.5. LC-MS: (ESI, m/z): [M+H] + = 916.5.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.27(d,J＝7.9Hz,1H),8.21(s,1H),7.70-7.58(m,3H),7.52(d,J＝8.7Hz,2H),7.37(dd,J＝8.2,1.8Hz,1H),6.90(s,1H),6.86(s,1H),6.70(s,1H),5.64–5.43(m,3H),3.79–3.69(m,1H),3.59-3.45(m,3H),3.28–3.20(m,2H),3.17-3.07(m,2H),2.98-2.86(m,4H),2.77–2.70(m,2H),2.69–2.56(m,1H),2.38(s,3H),2.26-2.14(m,2H),1.92–1.77(m,4H),1.74-1.63(m,2H),1.56–1.20(m,12H),1.14-0.94(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s, 1H), 8.27(d, J=7.9Hz, 1H), 8.21(s, 1H), 7.70-7.58(m, 3H), 7.52( d, J=8.7Hz, 2H), 7.37(dd, J=8.2, 1.8Hz, 1H), 6.90(s, 1H), 6.86(s, 1H), 6.70(s, 1H), 5.64–5.43(m ,3H),3.79-3.69(m,1H),3.59-3.45(m,3H),3.28-3.20(m,2H),3.17-3.07(m,2H),2.98-2.86(m,4H),2.77 –2.70(m,2H),2.69-2.56(m,1H),2.38(s,3H),2.26-2.14(m,2H),1.92-1.77(m,4H),1.74-1.63(m,2H) ,1.56-1.20(m,12H),1.14-0.94(m,4H).
实施例78：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 78: 1-(5-(9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)benzene)) yl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-aza Spiro[5.5]undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：9-((4-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的制备Step 1: 9-((4-((1R,4R)-4-(2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl) )ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecane Preparation of benzyl alkane-3-carboxylate
Figure PCTCN2022088560-appb-001026
Figure PCTCN2022088560-appb-001026
将(1R,4R)-4-(2-甲基-4-((1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羧酸(170mg,0.337mmol)，HATU(192mg,0.505mmol)和DIEA(130mg,1.01mmol)加入到9-(哌嗪-1-基甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的DMF(30mL)溶液中，室温搅拌过夜，反应液用水稀释(50mL)，二氯甲烷(50mL×3)萃取，粗品经反相柱层析(ACN:H 2O＝1:2)纯化得到9-((4-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯。 (1R,4R)-4-(2-methyl-4-((1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4- d] pyrimidin-6-yl)cyclohexane-1-carboxylic acid (170 mg, 0.337 mmol), HATU (192 mg, 0.505 mmol) and DIEA (130 mg, 1.01 mmol) were added to 9-(piperazin-1-ylmethyl) base)-3-azaspiro[5.5]undecane-3-carboxylate benzyl ester in DMF (30 mL) solution, stirred at room temperature overnight, the reaction solution was diluted with water (50 mL), extracted with dichloromethane (50 mL×3) , the crude product was purified by reverse phase column chromatography (ACN:H 2 O=1:2) to obtain 9-((4-((1R,4R)-4-(2-methyl-4-(((R)- 1-(3-Nitro-5-(trifluoromethyl)phenyl)ethyl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazine- 1-yl)methyl)-3-azaspiro[5.5]undecan-3-carboxylate benzyl ester.
LC-MS:(ESI,m/z):[M+H] +＝871.6. LC-MS: (ESI, m/z): [M+H] + = 871.6.
步骤2：9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯的制备Step 2: 9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino) -2-Methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecane - Preparation of benzyl 3-carboxylate
Figure PCTCN2022088560-appb-001027
Figure PCTCN2022088560-appb-001027
将9-((4-((1R,4R)-4-(2-甲基-4-(((R)-1-(3-硝基-5-(三氟甲基)苯基)乙基)氨基)吡啶并[3,4-d]嘧啶-6-基)环 己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(240mg,0.276mmol)溶于乙醇(20mL)，加入Raney-Ni(水悬浮物,0.3mL)和水合肼一水合物(85％,0.5mL)，反应液室温搅拌1小时，过滤，减压浓缩，得到粗品9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯。9-((4-((1R,4R)-4-(2-methyl-4-(((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl yl)amino)pyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan- Benzyl 3-carboxylate (240 mg, 0.276 mmol) was dissolved in ethanol (20 mL), Raney-Ni (water suspension, 0.3 mL) and hydrazine hydrate monohydrate (85%, 0.5 mL) were added, and the reaction solution was stirred at room temperature for 1 hours, filtered and concentrated under reduced pressure to give crude 9-((4-((1R,4R)-4-(4-((((R)-1-(3-amino-5-(trifluoromethyl)benzene)) yl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-aza Benzyl spiro[5.5]undecane-3-carboxylate.
LC-MS:(ESI,m/z):[M+H] +＝841.6. LC-MS: (ESI, m/z): [M+H] + = 841.6.
步骤3：(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己基)甲酮的制备Step 3: (4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R )-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexyl)methanone preparation
Figure PCTCN2022088560-appb-001028
Figure PCTCN2022088560-appb-001028
将9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羧酸苄酯(220mg,0.262mmol)溶于乙酸乙酯(20mL)，加入Pd(OH) 2(44mg,20％)，反应液在H 2氛围下70℃搅拌过夜，过滤，减压浓缩，得到粗品(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己基)甲酮。 9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2 -Methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3 -Benzyl carboxylate (220 mg, 0.262 mmol) was dissolved in ethyl acetate (20 mL), Pd(OH) 2 (44 mg, 20%) was added, the reaction solution was stirred at 70 °C overnight under H 2 atmosphere, filtered, and concentrated under reduced pressure , the crude product (4-((3-azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R )-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexyl)methanone .
LC-MS:(ESI,m/z):[M+H] +＝707.4. LC-MS: (ESI, m/z): [M+H] + = 707.4.
步骤4：1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 4: 1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl) )ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro Preparation of [5.5]Undecane-3-carbonyl)-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-001029
Figure PCTCN2022088560-appb-001029
将(4-((3-氮杂螺[5.5]十一烷-9-基)甲基)哌嗪-1-基)((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己基)甲酮(200mg,0.283mmol)用DMSO(20mL)溶解，分别加入perfluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate(147mg,0.338mmol)和DIEA(110mg,0.853mmol)，反应液室温搅拌过夜，用水稀释(50mL)，二氯甲烷萃取(50mL×3)，有机相减压浓缩，粗品使用反相制备纯化得到1-(5-(9-((4-((1R,4R)-4-(4-(((R)-1-(3-氨基-5-(三氟甲基)苯基)乙基)氨基)-2-甲基吡啶并[3,4-d]嘧啶-6-基)环己烷-1-羰基)哌嗪-1-基)甲基)-3-氮杂螺[5.5]十一烷-3-羰基)-2-氯苯基)二氢嘧啶-2,4(1H,3H)-二酮。(4-((3-Azaspiro[5.5]undecan-9-yl)methyl)piperazin-1-yl)((1R,4R)-4-(4-((((R)- 1-(3-Amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylpyrido[3,4-d]pyrimidin-6-yl)cyclohexyl)methanone (200 mg , 0.283mmol) was dissolved in DMSO (20mL), perfluorophenyl 4-chloro-3-(2,4-dioxotetrahydropyrimidin-1(2H)-yl)benzoate (147mg, 0.338mmol) and DIEA (110mg, 0.853mmol) were added respectively, The reaction solution was stirred at room temperature overnight, diluted with water (50 mL), extracted with dichloromethane (50 mL×3), the organic phase was concentrated under reduced pressure, and the crude product was purified by reverse-phase preparation to obtain 1-(5-(9-((4-((1R ,4R)-4-(4-(((R)-1-(3-amino-5-(trifluoromethyl)phenyl)ethyl)amino)-2-methylpyrido[3,4- d]pyrimidin-6-yl)cyclohexane-1-carbonyl)piperazin-1-yl)methyl)-3-azaspiro[5.5]undecan-3-carbonyl)-2-chlorophenyl) Dihydropyrimidine-2,4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝957.4. LC-MS: (ESI, m/z): [M+H] + = 957.4.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.91(s,1H),8.58(d,J＝7.9Hz,1H),8.19(s,1H),8.10(s,1H),7.63(d,J＝8.2Hz,1H),7.55(d,J＝1.9Hz,1H),7.39(dd,J＝8.2,1.9Hz,1H),6.89(s,1H),6.85(s,1H),6.71(s,1H),5.61–5.47(m,3H),3.78–3.72(m,1H),3.64–3.56(m,3H),3.54-3.41(m,6H),3.30-3.24(m,2H),2.82-2.71(m,3H),2.70-2.61(m,1H),2.43(s,3H),2.36-2.21(m,4H),2.17-2.07(m,2H),2.04–1.98(m,2H),1.85-1.71(m,2H),1.77-1.31(m,18H),1.16-0.90(m,4H). 1 H NMR (400MHz, DMSO-d 6 )δ10.51(s, 1H), 8.91(s, 1H), 8.58(d, J=7.9Hz, 1H), 8.19(s, 1H), 8.10(s, 1H), 7.63(d, J＝8.2Hz, 1H), 7.55(d, J＝1.9Hz, 1H), 7.39(dd, J＝8.2, 1.9Hz, 1H), 6.89(s, 1H), 6.85( s, 1H), 6.71 (s, 1H), 5.61–5.47 (m, 3H), 3.78–3.72 (m, 1H), 3.64–3.56 (m, 3H), 3.54–3.41 (m, 6H), 3.30- 3.24(m, 2H), 2.82-2.71(m, 3H), 2.70-2.61(m, 1H), 2.43(s, 3H), 2.36-2.21(m, 4H), 2.17-2.07(m, 2H), 2.04-1.98(m,2H),1.85-1.71(m,2H),1.77-1.31(m,18H),1.16-0.90(m,4H).
实施例79：1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮Example 79: 1-(2-Chloro-5-(4-(3-(1-((1R,4R)-4-(4-((((R)-1-(4-(2-chloro- 6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1 -Carbonyl)piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
步骤1：1-(2-氯-5-(4-(3-(哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 1: 1-(2-Chloro-5-(4-(3-(piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H )-dione preparation
Figure PCTCN2022088560-appb-001030
Figure PCTCN2022088560-appb-001030
将1,3-二(哌啶-4-基)丙烷(193.5mg,0.92mmol)和DIEA(178mg,1.38mmol)溶于DMSO(10mL)中，加入4-氯-3-(2,4-二氧代四氢嘧啶-1(2H)-基)苯甲酸五氟苯酯(200mg,0.46mmol)，室温反应30min。用水(30mL)稀释，乙酸乙酯(30mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用柱层析(MeOH:DCM＝1:9,流速40ml/min)纯化得到1-(2-氯-5-(4-(3-(哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。1,3-Di(piperidin-4-yl)propane (193.5 mg, 0.92 mmol) and DIEA (178 mg, 1.38 mmol) were dissolved in DMSO (10 mL) and 4-chloro-3-(2,4- Dioxotetrahydropyrimidin-1(2H)-yl)pentafluorophenyl benzoate (200 mg, 0.46 mmol) was reacted at room temperature for 30 min. Diluted with water (30 mL), extracted with ethyl acetate (30 mL×3), the organic phase was washed with saturated brine (40 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was subjected to column chromatography (MeOH:DCM=1:9 , flow rate 40ml/min) and purified to obtain 1-(2-chloro-5-(4-(3-(piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2, 4(1H,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝461.2. LC-MS: (ESI, m/z): [M+H] + = 461.2.
步骤2：1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮的制备Step 2: 1-(2-Chloro-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6 -((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1- Preparation of carbonyl)piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione
Figure PCTCN2022088560-appb-001031
Figure PCTCN2022088560-appb-001031
将(1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羧酸(100mg,0.17mmol)，1-(2-氯-5-(4-(3-(哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮(80mg,0.17mmol)和DIEA(65.8mg,0.51mmol)用DMF(5mL)溶解，最后加入HATU(77.5mg,0.20mmol)，反应液室温搅拌30min，用水(20mL)稀释，乙酸乙酯(20mL×3)萃取，有机相用饱和食盐水(40mL)洗，无水硫酸钠干燥，减压浓缩，粗品使用prep-HPLC纯化得到1-(2-氯-5-(4-(3-(1-((1R,4R)-4-(4-(((R)-1-(4-(2-氯-6-((二甲基氨基)甲基)苯基)噻吩-2-基)乙基)氨基)-7-甲氧基-2-甲基喹唑啉-6-基)环己烷-1-羰基)哌啶-4-基)丙基)哌啶-1-羰基)苯基)二氢嘧啶-2,4(1H,3H)-二酮。(1R,4R)-4-(4-(((R)-1-(4-(2-chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl (yl)amino)-7-methoxy-2-methylquinazolin-6-yl)cyclohexane-1-carboxylic acid (100 mg, 0.17 mmol), 1-(2-chloro-5-(4- (3-(piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H,3H)-dione (80 mg, 0.17 mmol) and DIEA (65.8 mg) , 0.51 mmol) was dissolved in DMF (5 mL), finally HATU (77.5 mg, 0.20 mmol) was added, the reaction solution was stirred at room temperature for 30 min, diluted with water (20 mL), extracted with ethyl acetate (20 mL×3), and the organic phase was saturated brine (40 mL) washed, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the crude product was purified by prep-HPLC to obtain 1-(2-chloro-5-(4-(3-(1-((1R,4R)-4-( 4-(((R)-1-(4-(2-Chloro-6-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)amino)-7-methoxy -2-Methylquinazolin-6-yl)cyclohexane-1-carbonyl)piperidin-4-yl)propyl)piperidine-1-carbonyl)phenyl)dihydropyrimidine-2,4(1H ,3H)-dione.
LC-MS:(ESI,m/z):[M+H] +＝1035.5. LC-MS: (ESI, m/z): [M+H] + = 1035.5.
1H NMR(400MHz,DMSO-d 6)δ10.51(s,1H),8.31(d,J＝8.1Hz,1H),8.05(s,1H),7.63(d,J＝8.2Hz,1H),7.54(d,J＝1.6Hz,1H),7.43-7.35(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.05-5.83(m,1H),4.52-4.35(m,2H),3.95-3.80(m,4H),3.80-3.69(m,1H),3.67-3.50(m,2H),3.20-3.08(m,2H),3.06-2.87(m,3H),2.83-2.70(m,3H),2.68-2.57(m,1H),2.42(s,3H),2.01(s,6H),1.92-1.39(m,18H),1.36-1.15(m,6H),1.13-0.82(m,4H). 1 H NMR (400MHz, DMSO-d 6 ) δ 10.51 (s, 1H), 8.31 (d, J=8.1 Hz, 1H), 8.05 (s, 1H), 7.63 (d, J=8.2 Hz, 1H) ,7.54(d,J＝1.6Hz,1H),7.43-7.35(m,4H),7.24(s,1H),7.02(s,1H),6.96(s,1H),6.05-5.83(m,1H) ), 4.52-4.35(m, 2H), 3.95-3.80(m, 4H), 3.80-3.69(m, 1H), 3.67-3.50(m, 2H), 3.20-3.08(m, 2H), 3.06-2.87 (m,3H),2.83-2.70(m,3H),2.68-2.57(m,1H),2.42(s,3H),2.01(s,6H),1.92-1.39(m,18H),1.36-1.15 (m,6H),1.13-0.82(m,4H).
Ⅱ生物活性测试实施例II Biological Activity Test Example
测试实施例1：KRAS-G12C/SOS1结合试验Test Example 1: KRAS-G12C/SOS1 binding assay
以下方法用于测定本发明优选化合物在体外条件下对KRAS-G12C/SOS1结合抑制程度。本方法使用KRAS-G12C/SOS1结合试验试剂盒(Cisbio,63ADK000CB16PEG)，以均相时间分辨荧光技术(HTRF)测定优选化合物对KRAS-G12C/SOS1结合竞争抑制测定。The following method was used to determine the degree of inhibition of KRAS-G12C/SOS1 binding by preferred compounds of the present invention under in vitro conditions. This method uses the KRAS-G12C/SOS1 binding assay kit (Cisbio, 63ADK000CB16PEG) to determine the competitive inhibition assay of KRAS-G12C/SOS1 binding by the preferred compounds by homogeneous time-resolved fluorescence (HTRF).
实验流程如下(详细方法参考试剂盒说明书)：将本发明中的化合物先溶解于DMSO中，浓度为20mM，用试剂盒中的缓冲液进行等梯度稀释，使受试化合物在反应体系中的终浓度范围为10000nM～0.04nM，DMSO的终浓度为0.5％。将2μL化合物与4μL 1x Tag1-SOS1、4μL 1xTag2-KRAS-G12C(含10μM三磷酸鸟苷,GTP)在25℃下孵育15min，随后向反应体系中加入5μL 1x Anti-Tag1-Tb3+以及5μL 1x Anti-Tag2-XL665在冰上下孵育3h。孵育结束后，在酶标仪EnVision(PerkinElmer,2105)上以HTRF模式测定各孔在激发波长为337nm，读取各孔在发射波长为620nm和665nm的荧光强度，使用公式Ratio＝(665nm/620nm)×104算出Ratio值。通过与对照组荧光强度比值进行对比，计算化合物在各浓度下的抑制率，进而通过GraphPad Prism 8以对数浓度-抑制率进行非线性曲线拟合，得出化合物的IC50值，见表1。The experimental procedure is as follows (refer to the kit instructions for the detailed method): first dissolve the compounds of the present invention in DMSO with a concentration of 20 mM, and perform isocratic dilution with the buffer in the kit to make the test compounds in the final reaction system. The concentration range was from 10000 nM to 0.04 nM, and the final concentration of DMSO was 0.5%. 2 μL of compound was incubated with 4 μL of 1x Tag1-SOS1, 4 μL of 1xTag2-KRAS-G12C (containing 10 μM guanosine triphosphate, GTP) for 15 min at 25°C, and then 5 μL of 1x Anti-Tag1-Tb3+ and 5 μL of 1x Anti were added to the reaction system. -Tag2-XL665 was incubated on ice for 3h. After the incubation, measure the excitation wavelength of each well at 337 nm in HTRF mode on a microplate reader EnVision (PerkinElmer, 2105), and read the fluorescence intensity of each well at emission wavelengths of 620 nm and 665 nm, using the formula Ratio=(665nm/620nm) )×104 to calculate the Ratio value. By comparing with the fluorescence intensity ratio of the control group, the inhibition rate of the compound at each concentration was calculated, and then the nonlinear curve fitting was performed by GraphPad Prism 8 with logarithmic concentration-inhibition rate, and the IC50 value of the compound was obtained, as shown in Table 1.
测试实施例2：SOS1降解试验Test Example 2: SOS1 Degradation Test
在KRAS G12C突变的人非小细胞肺癌细胞NCI-H358(ATCC或中国科学院干细胞库)、KRAS G12D突变的人肺癌细胞A-427(ATCC)、KRAS G12V突变的人结直肠腺癌细胞SW-620(ATCC)和KRAS G13D 突变的人结直肠腺癌上皮细胞DLD-1(ATCC)上考察化合物对SOS1的降解作用。具体方法为：KRAS G12C-mutated human non-small cell lung cancer cell NCI-H358 (ATCC or Chinese Academy of Sciences Stem Cell Bank), KRAS G12D-mutated human lung cancer cell A-427 (ATCC), KRAS G12V-mutated human colorectal adenocarcinoma cell SW-620 (ATCC) and KRAS G13D mutated human colorectal adenocarcinoma epithelial cells DLD-1 (ATCC) to investigate the degradation of SOS1 by compounds. The specific method is:
在24孔细胞培养板每孔中铺0.95mL细胞，使细胞密度为5×105个/孔；细胞板置于5％CO 2培养箱中37℃培养过夜。然后在相应铺有细胞的孔中加入50μL稀释后的化合物溶液，使化合物的终浓度在0.03～3000nM范围内。DMSO终浓度为0.25％。给药后的细胞板置于5％CO 2培养箱中37℃培养24h后，移除24孔中细胞培养液后，用1×PBS清洗2次，细胞培养板底部贴壁的NCI-H358细胞加入180μL RIPA(强)裂解液(碧云天,P0013B)，补充1mM苯甲基磺酰氟、蛋白酶抑制剂混合物(碧云天,P1008)以及蛋白酶磷酸酶抑制剂混合物(碧云天,P1045)裂解，冰上静置30min后，将每孔中的蛋白裂解液分别转移至1.5mL离心管中，15000g、4℃离心20min。离心后的细胞裂解上清液冻存于-80℃待测，用于WB方法检测SOS1蛋白降解水平。细胞裂解上清液中总蛋白浓度使用BCA蛋白质定量试剂盒(天根,PA115-02)测定。 Spread 0.95 mL of cells in each well of a 24-well cell culture plate to make the cell density 5×105 cells/well; place the cell plate in a 5% CO 2 incubator at 37°C overnight. Then, 50 μL of the diluted compound solution was added to the corresponding wells plated with cells to make the final concentration of the compound in the range of 0.03-3000 nM. The final concentration of DMSO was 0.25%. After administration, the cell plate was placed in a 5% CO 2 incubator at 37°C for 24 hours, the cell culture medium in the 24 wells was removed, and washed twice with 1×PBS. NCI-H358 cells adhered to the bottom of the cell culture plate. Add 180 μL RIPA (strong) lysis buffer (Biyuntian, P0013B), supplemented with 1 mM phenylmethylsulfonyl fluoride, protease inhibitor cocktail (Biyuntian, P1008) and protease phosphatase inhibitor cocktail (Biyuntian, P1045) lysis, ice After standing for 30 min, the protein lysate in each well was transferred to a 1.5 mL centrifuge tube, and centrifuged at 15,000 g and 4°C for 20 min. The cell lysate supernatant after centrifugation was frozen at -80°C for testing, and was used to detect the degradation level of SOS1 protein by WB method. The total protein concentration in the cell lysis supernatant was determined using BCA protein quantification kit (Tiangen, PA115-02).
测试实施例3：人SOS1蛋白免疫印迹试验Test Example 3: Human SOS1 Western Blot Assay
根据BCA检测细胞裂解液中总蛋白的浓度，用PBS和5×SDS-PAGE蛋白上样缓冲液(碧云天,P0015L)调整至0.5μg/μL，100℃水浴15min，然后置于冰上冰浴5min后，14000g、4℃离心1min，混匀作为WB的上样样品。用预制胶(凯基,KGMG010W15)做蛋白电泳，上样量为10μL(总蛋白5μg)，Tris-MOPS-SDS电泳液(Adamas,P1598253)后120V 55min恒压电泳，电泳结束后，恒流250mA 65min把胶条上的蛋白转至PVDF膜上。转膜结束后将膜放入1×QuickBlock封闭液(碧云天,P0235)中室温孵育30min。封闭结束后，PVDF膜分别进行SOS1一抗(Abcam,ab140621)孵育4℃过夜，TBST缓冲液(2.4g Tris,8.8g NaCl,1.5mL Tween 20,调pH至7.4，定容至1L)洗涤膜30min(10min/次)，二抗(Abcam,ab205718)室温孵育2h，TBST缓冲液洗涤膜30min(10min/次)，最后用Clarity Western ECL Substrate(BIO-RAD,170-5061)孵育5min发光显色，化学发光成像系统(勤翔,ChemiScope 6200 Touch)进行显色和蛋白图谱拍照。蛋白图谱通过勤翔化学发光分析软件进行灰度值分析。使用公式：灰度校正值＝(目的蛋白灰度值/对应内参灰度值)×103，计算出各样品的灰度校正值。再与对照组灰度校正值对比计算降解率。进而通过GraphPad Prism 8以对数浓度-抑制率进行非线性曲线拟合，得出化合物的DC50和Dmax值。The concentration of total protein in the cell lysate was detected by BCA, adjusted to 0.5 μg/μL with PBS and 5×SDS-PAGE protein loading buffer (Biyuntian, P0015L), water bathed at 100 °C for 15 min, and then placed on ice in an ice bath After 5 min, centrifuge at 14,000 g for 1 min at 4°C, and mix well to serve as the loading sample for WB. Use precast gel (Keygen, KGMG010W15) for protein electrophoresis, the loading volume is 10μL (total protein 5μg), Tris-MOPS-SDS electrophoresis solution (Adamas, P1598253), 120V 55min constant voltage electrophoresis, after electrophoresis, constant current 250mA After 65min, the protein on the strip was transferred to PVDF membrane. After transfer, the membrane was placed in 1×QuickBlock blocking solution (Biyuntian, P0235) and incubated at room temperature for 30min. After blocking, the PVDF membrane was incubated with SOS1 primary antibody (Abcam, ab140621) at 4°C overnight, and washed with TBST buffer (2.4g Tris, 8.8g NaCl, 1.5mL Tween 20, adjusted to pH 7.4, and the volume was adjusted to 1L). 30min (10min/time), the secondary antibody (Abcam, ab205718) was incubated at room temperature for 2h, the membrane was washed with TBST buffer for 30min (10min/time), and finally incubated with Clarity Western ECL Substrate (BIO-RAD, 170-5061) for 5min for luminescence and color development , chemiluminescence imaging system (Qinxiang, ChemiScope 6200 Touch) for color development and protein map photography. The protein map was analyzed by the Qinxiang chemiluminescence analysis software. Using the formula: grayscale correction value=(target protein grayscale value/corresponding internal reference grayscale value)×103, the grayscale correction value of each sample was calculated. The degradation rate was calculated by comparing with the grayscale correction value of the control group. Then, nonlinear curve fitting was performed with logarithmic concentration-inhibition rate by GraphPad Prism 8, and the DC50 and Dmax values of the compounds were obtained.
测试实施例4：3D细胞增殖抑制试验Test Example 4: 3D Cell Proliferation Inhibition Test
在KRAS G12C突变的人非小细胞肺癌细胞NCI-H358(ATCC或中国科学院干细胞库)、KRAS G12D突变的人转移胰腺腺癌细胞AsPC-1(ATCC)、KRAS G12V突变的人肺腺癌细胞NCI-H441(ATCC)和KRAS G13D突变的人结直肠腺癌上皮细胞DLD-1(ATCC)上考察化合物对3D细胞增殖的抑制作用。具体方法为：KRAS G12C-mutated human non-small cell lung cancer cell NCI-H358 (ATCC or Chinese Academy of Sciences Stem Cell Bank), KRAS G12D-mutated human metastatic pancreatic adenocarcinoma cell AsPC-1 (ATCC), KRAS G12V-mutated human lung adenocarcinoma cell NCI -H441 (ATCC) and KRAS G13D mutated human colorectal adenocarcinoma epithelial cells DLD-1 (ATCC) were used to investigate the inhibitory effect of compounds on 3D cell proliferation. The specific method is:
在384孔低吸附微孔板(Corning,3657)相应微孔中用Echo声波移液系统(Labcyte,Echo 550)加入200nL化合物梯度稀释溶液，使受试化合物在反应体系中的终浓度范围为20000nM～0.008nM。然后将40μL一定密度的细胞加入对应的微孔板中。除受试化合物测试孔外，同时设置DMSO对照孔和培养基对照孔，DMSO对照孔中含有DMSO和细胞，培养基孔中只含有培养基。加样完成后盖上板盖，将测384孔低吸附微孔板放入5％二氧化碳培养箱中，37℃孵育7天。7天后取出微孔板，每孔加入40μL CTG试剂(Promega,G9683)，室温孵育30分钟后在酶标仪EnVision上采用化学发光程序读数。通过细胞增殖抑制百分比计算公式：抑制率％＝(DMSO对照组平均值-化合物单浓度读值)/(DMSO对照组平均值-培养基对照组平均值)×100，计算化合物在各浓度时的抑制率，进而通过GraphPad Prism 8以对数浓度-抑制率进行非线性曲线拟合，得出化合物的IC50值。Add 200nL of compound gradient dilution solution to the corresponding microwell of 384-well low adsorption microplate (Corning, 3657) with Echo sonic pipetting system (Labcyte, Echo 550), so that the final concentration of the test compound in the reaction system is in the range of 20000nM ~0.008 nM. Then 40 μL of cells at a certain density were added to the corresponding microplates. In addition to the test compound test wells, DMSO control wells and medium control wells were set at the same time. The DMSO control wells contained DMSO and cells, and the medium wells contained only medium. After adding samples, cover the plate cover, put the 384-well low adsorption microplate into a 5% carbon dioxide incubator, and incubate at 37°C for 7 days. After 7 days, the microplate was taken out, and 40 μL of CTG reagent (Promega, G9683) was added to each well. After incubation at room temperature for 30 minutes, the microplate reader was read by chemiluminescence program on EnVision. Calculate the percentage of inhibition of cell proliferation by the formula: % inhibition rate = (average value of DMSO control group - reading value of a single concentration of compound)/(average value of DMSO control group - average value of medium control group) × 100, calculate the compound at each concentration Inhibition rate, and then through GraphPad Prism 8 to perform nonlinear curve fitting with logarithmic concentration-inhibition rate, and obtain the IC50 value of the compound.
表1Table 1
Figure PCTCN2022088560-appb-001032
Figure PCTCN2022088560-appb-001032
Figure PCTCN2022088560-appb-001033
Figure PCTCN2022088560-appb-001033
Figure PCTCN2022088560-appb-001034
Figure PCTCN2022088560-appb-001034
Figure PCTCN2022088560-appb-001035
Figure PCTCN2022088560-appb-001035
表2Table 2
Figure PCTCN2022088560-appb-001036
Figure PCTCN2022088560-appb-001036
表1和表2中：In Table 1 and Table 2:
“-”表示未检测；"-" means not detected;
当DC 50≤50nM为A，当50nM<DC 50≤100nM时为B，当100nM<DC 50≤500nM为C，当500nM<DC 50≤1000nM为D；1000nM<DC 50≤10μM为E； When DC 50 ≤50nM is A, when 50nM<DC 50 ≤100nM is B, when 100nM<DC 50 ≤500nM is C, when 500nM<DC 50 ≤1000nM is D; 1000nM<DC 50 ≤10μM is E;
当80≤D max(％)≤100时为A，当50≤D max(％)<80时为B，当30≤D max(％)<50时为C，当D max(％)<30时为D； A when 80≤D max (%)≤100, B when 50≤D max (%)<80, C when 30≤D max (%)<50, C when D max (%)<30 time is D;
当IC 50≤15nM为A，当15nM<IC 50≤30nM时为B，当30nM<IC 50≤50nM为C，当50nM<IC 50≤100nM为D，当100nM<IC 50≤1000nM为E。 A when IC 50 ≤15nM, B when 15nM<IC 50 ≤30nM, C when 30nM<IC 50 ≤50nM, D when 50nM<IC 50 ≤100nM, E when 100nM<IC 50 ≤1000nM.
实验结论：本发明化合物能够有效的与SOS1靶蛋白结合或产生抑制效果，本发明所述化合物能够有效的特异性的降解SOS1蛋白。Experimental conclusion: the compound of the present invention can effectively bind to or produce an inhibitory effect on the SOS1 target protein, and the compound of the present invention can effectively and specifically degrade the SOS1 protein.

Claims (28)

  1. 一种式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐：A compound of formula I, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceutically acceptable salts thereof :
    S-L-ES-L-E
    ⅠⅠ
    其中：in:
    S为能够抑制SOS1蛋白活性或与SOS1蛋白相结合的小分子化合物；S is a small molecule compound that can inhibit the activity of SOS1 protein or bind to SOS1 protein;
    L为连接链，其通过共价键连接S和E；L is the linking chain, which connects S and E by covalent bonds;
    E为E3泛素连接酶复合体的小分子配体。E is the small molecule ligand of the E3 ubiquitin ligase complex.
  2. 如权利要求1所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述S为S1、S1'、-X-S1'、S1”、-X-S1”、S2、S2'、-X-S2'、S2”、-X-S2”、S3、S4、S5、S5'或-X-S2”：X为O、NH或S，优选为O；The compound of formula I as claimed in claim 1, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceuticals An acceptable salt above, the S is S1, S1', -X-S1', S1", -X-S1", S2, S2', -X-S2', S2", -X-S2", S3, S4, S5, S5' or -X-S2": X is O, NH or S, preferably O;
    Figure PCTCN2022088560-appb-100001
    Figure PCTCN2022088560-appb-100001
    其中所述S1、S1'、S1”中：Wherein said S1, S1', S1":
    R 1选自氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、C 1-C 6卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、C 3-C 8环烷基或-C 4-C 8环烯基； R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8 cycloalkenyl;
    R 1为-NS(O)(R d)(R e)，所述C 1-C 6和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、6-10元芳基或5-10元杂芳基； R 1 is -NS(O)(R d )(R e ), and the C 1 -C 6 and Re are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 - C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 6-10 membered aryl or 5-10 membered heteroaryl;
    R 1为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b，所述R a和R b各自独立的为氢、-C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1为-NH-(CH 2) k-NH-C(O)-R aa，所述R aa为C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基，且k为1或者2； R 1 is -NH-(CH 2 ) k -NH-C(O)-R aa , wherein R aa is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl, and k is 1 or 2;
    R 1为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
    此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO2, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered heterocycle Alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, - (CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b group substitution; said R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯 基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
    或者R 1为 or R 1 as
    Figure PCTCN2022088560-appb-100002
    Figure PCTCN2022088560-appb-100003
    或者
    Figure PCTCN2022088560-appb-100004
    Figure PCTCN2022088560-appb-100002
    Figure PCTCN2022088560-appb-100003
    or
    Figure PCTCN2022088560-appb-100004
    或者相邻2个R 1与它们各自连接的碳原子一起形成5-7元环烷基或5-7元杂环烷基； Or adjacent 2 R 1 together with the carbon atoms to which they are attached to form a 5-7 membered cycloalkyl or 5-7 membered heterocycloalkyl;
    且所述x为1、2或者3；and said x is 1, 2 or 3;
    A 1为C 4-C 12环烷基、杂环烷基、芳基或杂芳基； A 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl;
    R 2为氢、-OH、氧代、卤素、-CN、C 1-C 6烷基、C 1-C 6烷氧基、C 2-C 6烯基、-C 2-C 6炔基、-C 3-C 8环烷基、-C 3-C 8环烷氧基、-C 3-C 8卤代环烷氧基、-C 4-C 8环烯基、4-7元杂环烷基、-O-CH 2-4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、-C 1-C 6卤代烷基、-C 1-C 6卤代烷氧基、-C 1-C 6烷基磺酰基； R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6 alkylsulfonyl;
    R 2为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基或-C(O)C 1-C 3烷基； R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl or -C(O)C 1 -C 3 alkyl;
    R 2为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -C(O)NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
    R 2为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
    R 2为-OR h；所述R h为C 1-C 6烷基； R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
    R 2为-(CH 2)NR aR b，所述R a和R b各自独立的氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkane base;
    且w为1、2、3或4；and w is 1, 2, 3 or 4;
    所述A 2(R 3) Y为氢； The A 2 (R 3 ) Y is hydrogen;
    或者A 2为C 4-C 12环烷基、杂环烷基、芳基或杂芳基，且 or A 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl, and
    R 3为氢、卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、C 7-C 8环炔基、4-7元杂环烷基、5-10元杂环烯基、苯基、杂芳基、C 1-C 6卤代烷基； R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 7 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
    所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-C 1-C 6烷基、-C 1-C 6烷氧基、-C 1-C 6卤代烷基、苯基、杂芳基或-C(O)NR iR j的取代基取代，所述R i和R j各自独立的为氢或者C 1-C 6烷基； The alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
    或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR kR l取代，所述R k和R l各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 1-C 6烷基磺酰基、苯基、杂芳基、-CH 2-C(O)-R m、-C(O)R p或4-7元杂环烷基，且所述烷基、炔基、烯基、环烷基、苯基、杂芳基和杂环烷基各自独立的任选的被1个、2个或3个选自C 1-C 6卤代烷基、-OH、氧代基、苯基、-CN、C 1-C 6烷氧基或杂芳基取代，且所述杂芳基任选被甲基取代；且所述R m为双环杂芳基、C 1-C 6烷氧基或者-NR nR o，所述R n和R o各自独立的为氢、C 1-C 6烷基或者苯基，所述烷基任选被C 1-C 6烷氧基或者苯基取代，或者-NR nR o为4-7元氮杂环烷基，所述氮杂环烷基通过N原子连接分子其他部位，且还包含1个或者多个选自N或者O的杂原子；所述R p选自C 1-C 6烷氧基、任选被1个、2个或者3个选自-OH或 者C 1-C 6烷氧基取代的C 1-C 6烷基、单环或双环杂芳基、4-7元杂环烷基或者R p为-CH 2-NR qR r，所述R q和R r各自独立的选自氢、苯基或者任选被F取代的C 1-C 6烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl , the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1 - C6 haloalkyl, -OH, oxo base, phenyl, -CN, C 1 -C 6 alkoxy or heteroaryl substituted, and the heteroaryl is optionally substituted with methyl; and the R m is bicyclic heteroaryl, C 1 -C 6 alkoxy or -NR n R o , said R n and R o are each independently hydrogen, C 1 -C 6 alkyl or phenyl, said alkyl optionally being C 1 -C 6 alkoxy Or phenyl substituted, or -NR n R o is a 4-7 membered azacycloalkyl, the azacycloalkyl is connected to other parts of the molecule through an N atom, and also contains 1 or more selected from N or O The heteroatom; the R p is selected from C 1 -C 6 alkoxy, C 1 -C 6 optionally substituted by 1 , 2 or 3 selected from -OH or C 1 -C 6 alkoxy Alkyl, monocyclic or bicyclic heteroaryl, 4-7 membered heterocycloalkyl or R p is -CH 2 -NR q R r , said R q and R r are each independently selected from hydrogen, phenyl or any Select C 1 -C 6 alkyl substituted by F;
    或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR sR t取代，所述-NR sR t为通过氮原子连接至分子其他部位的4-7元氮杂环烷基或者通过氮原子连接至分子其他部位的6-10元氮螺杂环烷基，且进一步包括最多两个选自N或者O的杂原子，且任选的被1个、2个或者3个选自-OH、氧代基、C 1-C 6烷基、C 1-C 6羟基烷基、-C(O)OR z的取代基取代，所述R z为C 1-C 6烷基、卤素、-N(C 1-C 6烷基) 2、-CH 2N(C 1-C 6烷基) 2、-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt , the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 alkyl) 2 , -CH 2 N(C 1 - C 6 alkyl) 2 , -C(O)NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    或者R 3为C(O)R v、-C(O)NH 2、-C(O)NHR v、-C(O)NR vR w、-C(O)OR v，所述R v和R w各自独立的为氢、C 1-C 4烷基、C 1-C 4卤代烷基、苯基或者-(CH 2) 2NR xR y，所述R x和R y各自独立的为氢、C 1-C 4烷基或者-(CH 2) 2N(CH 3) 2； or R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 N(CH 3 ) 2 ;
    或者R 3为-NH 2、-NHR z、-NR zR za、-NHC(O)R z、-NHC(O)OR z、-NHS(O) 2R z、4-7元杂环烷基、杂芳基、螺杂环烷基、稠杂环烷基、桥杂环烷基，所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； Or R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)OR z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
    或者R 3为C 1-C 6烷氧基、C 1-C 6卤代烷氧基、-O(CH 2) s-C 3-C 8环烷基、-O(CH 2) s-苯基、-O(CH 2) s-杂环烷基、-O(CH 2) s-杂芳基，所述s为0、1、2或者3； Or R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
    或者R 3为-S(O) 2R z、-S(O) 2NH 2、-S(O) 2NHR z、-S(O) 2NR zR za,所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基，所述y为0、1、2或者3； or R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl, and said y is 0, 1, 2 or 3;
    Y为0、1、2、3、4或5；Y is 0, 1, 2, 3, 4 or 5;
    L'为键、-(CH 2) k-、-O(CH 2) k-、-(CH 2) k-O-或者-O-(CH 2) k-O-，所述k为0、1、2或者3，或者L'为-CH＝CH-(CH 2) n-,所述n为0、1或者2； L' is a bond, -(CH 2 ) k -, -O(CH 2 ) k -, -(CH 2 ) k -O- or -O-(CH 2 ) k -O-, wherein k is 0, 1, 2 or 3, or L' is -CH=CH-(CH 2 ) n -, and the n is 0, 1 or 2;
    R 4、R 5各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代； R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace;
    Figure PCTCN2022088560-appb-100005
    Figure PCTCN2022088560-appb-100005
    其中所述S2、S2'、S2”中：Wherein said S2, S2', S2":
    R 1为氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b；所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkyl mercapto or -NR a R b ; the R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、C 1-C 6卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、C 3-C 8环烷基或-C 4-C 8环烯基； R 1 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8 cycloalkenyl;
    R 1为-NS(O)(R d)(R e)，所述R d和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基； R 1 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl;
    R 1为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b,所述R a和R b各自独立的为氢、-C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 1 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1为-NH-(CH 2) k-NH-C(O)-(C 1-C 6烷基)，所述k为1或者2； R 1 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
    R 1为-NH-(CH 2) i-R f，所述i为0、1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 1 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
    此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b The group is substituted; the R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 1为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 1 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
    或者R 1为 or R 1 as
    Figure PCTCN2022088560-appb-100006
    Figure PCTCN2022088560-appb-100007
    所述L 2a为C(O),L 2b为键或C 1-C 6亚烷基，X 2为
    Figure PCTCN2022088560-appb-100006
    Figure PCTCN2022088560-appb-100007
    Described L 2 a is C(O), L 2 b is bond or C 1 -C 6 alkylene, X 2 is
    Figure PCTCN2022088560-appb-100008
    Rx 2为
    Figure PCTCN2022088560-appb-100009
    Figure PCTCN2022088560-appb-100008
    Rx 2 is
    Figure PCTCN2022088560-appb-100009
    或者R 1为 or R 1 as
    Figure PCTCN2022088560-appb-100010
    Figure PCTCN2022088560-appb-100011
    或者
    Figure PCTCN2022088560-appb-100012
    Figure PCTCN2022088560-appb-100010
    Figure PCTCN2022088560-appb-100011
    or
    Figure PCTCN2022088560-appb-100012
    或者相邻2个R 1与它们各自连接的碳原子一起形成5-7元环烷基或5-7元杂环烷基； Or adjacent 2 R 1 together with the carbon atoms to which they are attached to form a 5-7 membered cycloalkyl or 5-7 membered heterocycloalkyl;
    且所述x为1、2、3或者4；and said x is 1, 2, 3 or 4;
    A 1为C 4-C 12环烷基、杂环烷基、芳基或杂芳基； A 1 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl;
    R 2为氢、-OH、氧代、卤素、-CN、C 1-C 6烷基、C 1-C 6烷氧基、C 2-C 6烯基、-C 2-C 6炔基、-C 3-C 8环烷基、-C 3-C 8环烷氧基、-C 3-C 8卤代环烷氧基、-C 4-C 8环烯基、4-7元杂环烷基、-O-CH 2-4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、-C 1-C 6卤代烷基、-C 1-C 6卤代烷氧基、-C 1-C 6烷基磺酰基； R 2 is hydrogen, -OH, oxo, halogen, -CN, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, - C 2 -C 6 alkynyl, -C 3 -C 8 cycloalkyl, -C 3 -C 8 cycloalkoxy, -C 3 -C 8 halocycloalkoxy, -C 4 -C 8 cycloalkenyl, 4-7 membered heterocycle Alkyl, -O-CH 2 -4-7-membered heterocycloalkyl, 5-10-membered heterocycloalkenyl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl base, -C 1 -C 6 haloalkyl, -C 1 -C 6 haloalkoxy, -C 1 -C 6 alkylsulfonyl;
    R 2为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 2为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
    R 2为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 2 is -C(O)OR g , said R g is hydrogen or C 1 -C 6 alkyl;
    R 2为-OR h；所述R h为C 1-C 6烷基； R 2 is -OR h ; Described R h is C 1 -C 6 alkyl;
    R 2为-(CH 2)NR aR b，所述R a和R b各自独立的氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -(CH 2 )NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkane base;
    且w为1、2、3或者4；and w is 1, 2, 3 or 4;
    所述A 2(R 3) Y为氢； The A 2 (R 3 ) Y is hydrogen;
    或者A 2为C 4-C 12环烷基、杂环烷基、芳基或杂芳基，且 or A 2 is C 4 -C 12 cycloalkyl, heterocycloalkyl, aryl or heteroaryl, and
    R 3为氢、卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、C 2-C 8环炔基、4-7元杂环烷基、5-10元杂环烯基、苯基、杂芳基、C 1-C 6卤代烷基； R 3 is hydrogen, halogen, -OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 ring Alkyl, C 4 -C 8 cycloalkenyl, C 2 -C 8 cycloalkynyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl;
    所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-C 1-C 6烷基、-C 1-C 6烷氧基、-C 1-C 6卤代烷基、苯基、杂芳基或-C(O)NR iR j的取代基取代，所述R i和R j各自独立的为氢或者C 1-C 6烷基； The alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted by 1, 2 or 3 selected from halogen, -OH, oxo, -CN, -C1 - C6 alkyl, -C1 - C6 alkoxy, -C1 - C6 haloalkyl, phenyl, heteroaryl or - Substituent substitution of C(O)NR i R j , each of said R i and R j is independently hydrogen or C 1 -C 6 alkyl;
    或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR kR l取代，所述R k和R l各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 1-C 6烷基磺酰基、苯基、杂芳基、-CH 2-C(O)-R m、-C(O)R p或4-7元杂环烷基，且所述烷基、炔基、烯基、环烷基、苯基、杂芳基和杂环烷基各自独立的任选的被1个、2个或3个选自C 1-C 6卤代烷基、-OH、氧代基、苯基、-CN、C 1-C 6烷氧基或杂芳基取代，且所述杂芳基任选被甲基取代；且所述R m为双环杂芳基、C 1-C 6烷氧基或者-NR nR o，所述R n和R o各自独立的为氢、C 1-C 6烷基或者苯基，所述烷基任选被C 1-C 6烷氧基或者苯基取代，或者-NR nR o为4-7元氮杂环烷基，所述氮杂环烷基通过N原子连接分子其他部位，且还包含1个或者多个选自N或者O的杂原子；所述R p选自C 1-C 6烷氧基、任选被1个、2个或者3个选自-OH或者C 1-C 6烷氧基取代的C 1-C 6烷基、单环或双环杂芳基、4-7元杂环烷基或者R p为-CH 2-NR qR r，所述R q和R r各自独立的选自氢、苯基或者任选被F取代的C 1-C 6烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRkRl , the R k and R l are each independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 1 - C 6 alkylsulfonyl, phenyl, heteroaryl, -CH 2 -C(O)-R m , -C(O)R p or 4-7 membered heterocycloalkyl, and the alkyl, alkyne alkenyl, alkenyl, cycloalkyl, phenyl, heteroaryl and heterocycloalkyl are each independently optionally selected from 1, 2 or 3 C1 - C6 haloalkyl, -OH, oxo base, phenyl, -CN, C 1 -C 6 alkoxy or heteroaryl substituted, and the heteroaryl is optionally substituted with methyl; and the R m is bicyclic heteroaryl, C 1 -C 6 alkoxy or -NR n R o , said R n and R o are each independently hydrogen, C 1 -C 6 alkyl or phenyl, said alkyl optionally being C 1 -C 6 alkoxy Or phenyl substituted, or -NR n R o is a 4-7 membered azacycloalkyl, the azacycloalkyl is connected to other parts of the molecule through an N atom, and also contains 1 or more selected from N or O The heteroatom; the R p is selected from C 1 -C 6 alkoxy, C 1 -C 6 optionally substituted by 1 , 2 or 3 selected from -OH or C 1 -C 6 alkoxy Alkyl, monocyclic or bicyclic heteroaryl, 4-7 membered heterocycloalkyl or R p is -CH 2 -NR q R r , said R q and R r are each independently selected from hydrogen, phenyl or any Select C 1 -C 6 alkyl substituted by F;
    或者所述烷基、烯基、炔基、环烷基、杂环烷基、芳基、杂芳基、环烯基、环炔基和杂环烯基任选的被-NR sR t取代，所述-NR sR t为通过氮原子连接至分子其他部位的4-7元氮杂环烷基或者通过氮原子连接至分子其他部位的6-10元氮螺杂环烷基，且进一步包括最多两个选自N或者O的杂原子，且任选的被1个、2个或者3个选自-OH、氧代基、C 1-C 6烷基、C 1-C 6羟基烷基、-C(O)OR z的取代基取代，所述R z为C 1-C 6烷基、卤素、-N(C 1-C 6烷基) 2、-CH 2N(C 1-C 6烷基) 2、-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； or the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkenyl, cycloalkynyl and heterocycloalkenyl are optionally substituted with -NRsRt , the -NR s R t is a 4-7-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom or a 6-10-membered aza-heterocycloalkyl connected to other parts of the molecule through a nitrogen atom, and further including up to two heteroatoms selected from N or O, optionally surrounded by 1, 2 or 3 selected from -OH, oxo, C1 - C6 alkyl, C1 - C6 hydroxyalkane group, -C(O)OR z substituent, the R z is C 1 -C 6 alkyl, halogen, -N(C 1 -C 6 alkyl) 2 , -CH 2 N(C 1 - C 6 alkyl) 2 , -C(O)NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    或者R 3为C(O)R v、-C(O)NH 2、-C(O)NHR v、-C(O)NR vR w、-C(O)OR v，所述R v和R w各自独立的为氢、C 1-C 4烷基、C 1-C 4卤代烷基、苯基或者-(CH 2) 2NR xR y，所述R x和R y各自独立的为氢、C 1-C 4烷基或者-(CH 2) 2NH(CH 3) 2； or R 3 is C(O)R v , -C(O)NH 2 , -C(O)NHR v , -C(O)NR v R w , -C(O)OR v , said R v and R w is each independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, phenyl or -(CH 2 ) 2 NR x R y , said R x and R y are each independently hydrogen , C 1 -C 4 alkyl or -(CH 2 ) 2 NH(CH 3 ) 2 ;
    或者R 3为-NH 2、-NHR z、-NR zR za、-NHC(O)R z、-NHC(O)OR z、-NHS(O) 2R z、4-7元杂环烷基、杂芳基、螺杂环烷基、稠杂环烷基、桥杂环烷基，所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； Or R 3 is -NH 2 , -NHR z , -NR z R za , -NHC(O)R z , -NHC(O)OR z , -NHS(O) 2 R z , 4-7 membered heterocycloalkane base, heteroaryl, spiroheterocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, the R z and R za are each independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
    或者R 3为C 1-C 6烷氧基、C 1-C 6卤代烷氧基、-O(CH 2) s-C 3-C 8环烷基、-O(CH 2) s-苯基、-O(CH 2) s-杂环烷基、-O(CH 2) s-杂芳基，所述s为0、1、2或者3； Or R 3 is C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, -O(CH 2 ) s -C 3 -C 8 cycloalkyl, -O(CH 2 ) s -phenyl, -O(CH 2 ) s -heterocycloalkyl, -O(CH 2 ) s -heteroaryl, wherein s is 0, 1, 2 or 3;
    或者R 3为-S(O) 2R z、-S(O) 2NH 2、-S(O) 2NHR z、-S(O) 2NR zR za,所述R z和R za各自独立的为C 1-C 4烷基、C 1-C 4卤代烷基或者苯基； or R 3 is -S(O) 2 R z , -S(O) 2 NH 2 , -S(O) 2 NHR z , -S(O) 2 NR z R za , each of said R z and R za independently C 1 -C 4 alkyl, C 1 -C 4 haloalkyl or phenyl;
    Y为0、1、2、3、4或5；Y is 0, 1, 2, 3, 4 or 5;
    L'为键、-(CH 2) k-、-O(CH 2) k-、-(CH 2) k-O-或者-O-(CH 2) k-O-，所述k为0、1、2或者3，或者L'为-CH＝CH- (CH 2) n-,所述n为0、1或者2； L' is a bond, -(CH 2 ) k -, -O(CH 2 ) k -, -(CH 2 ) k -O- or -O-(CH 2 ) k -O-, wherein k is 0, 1, 2 or 3, or L' is -CH=CH- (CH 2 ) n -, and the n is 0, 1 or 2;
    R 4、R 5各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代； R 4 and R 5 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace;
    T和V都为N，或者T为C，V为N，或者T为N，V为C；Both T and V are N, or T is C and V is N, or T is N and V is C;
    Figure PCTCN2022088560-appb-100013
    Figure PCTCN2022088560-appb-100013
    其中所述S3中：where the S3:
    Q 1和Q 2各自独立的CH或者N； Q 1 and Q 2 are each independent CH or N;
    Q 3、Q 4和Q 7各自独立的为C或者N，所述Q 3和Q 4至少有一个为C，所述Q 3、Q 4和Q 7不全部为N； Q 3 , Q 4 and Q 7 are independently C or N, at least one of said Q 3 and Q 4 is C, and not all of said Q 3 , Q 4 and Q 7 are N;
    Q 5为CH、N、NH、O或者S； Q 5 is CH, N, NH, O or S;
    Q 6为CH、N、NH、N(C 1-C 6烷基)、N(C 1-C 6杂烷基)、N(3-7元环烷基)、N(3-7元杂环)、O或者S； Q 6 is CH, N, NH, N(C 1 -C 6 alkyl), N(C 1 -C 6 heteroalkyl), N(3-7 membered cycloalkyl), N(3-7 membered heteroalkyl) ring), O or S;
    所述Q 1、Q 2、Q 3、Q 4、Q 5、Q 6和Q 7中至少有一个为N、NH、O或者S； At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 , Q 6 and Q 7 is N, NH, O or S;
    R 1选自氢、C 1-C 6烷基、C 1-C 6烷氧基、卤素、-NHR 1a、-OR 1a、C 3-C 6环烷基、C 3-C 6环烷氧基或者-CN；所述C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基和C 3-C 6环烷氧基任选的被选自卤素、-NHR 1a或-OR 1a的取代基取代；所述R 1a为氢、C 1-C 6烷基、3-6元杂环或者C 1-C 6卤代烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, halogen, -NHR 1a , -OR 1a , C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or -CN; the C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl and C 3 -C 6 cycloalkoxy are optionally selected from halogen, Substituent substitution of -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
    L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-S(O)-、-S(＝O)(＝NH)-、-S(＝O)[＝N(C 1-C 6烷基)]-、-N(C 1-C 6烷基)-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -S(O)-, - S(=O)(=NH)-, -S(=O)[=N(C 1 -C 6 alkyl)]-, -N(C 1 -C 6 alkyl)-, -C(O) (CH 2 ) p -, -(CH 2 ) p - or O; the o is 0, 1 or 2; the p is an integer from 1 to 6;
    R 2选自氢、卤素、-CN、-NO 2、C 1-C 6烷基巯基、C 2-C 6炔基、C 1-C 6烷基、C 2-C 6烯基、-NR 2bR 2c、-OR 2a、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述C 1-C 6烷基、C 2-C 6烯基、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、C 1-C 6卤代烷基、-OH、-OR 2a、氧代基、卤素、-C(O)R 2a、-C(O)OR 2a、-C(O)NR 2bR 2c、-CN、-NR 2bR 2c、3-6元环烷基、3-7元杂环烷基、6-10元芳基或5-10元杂芳基的取代基取代；所述R 2a为氢、C 1-C 6烷基、C 1-C 6卤代烷基、3-7元杂环烷基、或者-(CH 2) rOCH 3，所述r为1、2或者3； R 2 is selected from hydrogen, halogen, -CN, -NO 2 , C 1 -C 6 alkylmercapto, C 2 -C 6 alkynyl, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, -NR 2b R 2c , -OR 2a , 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-10-membered heteroaryl; the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5- The 10-membered heteroaryl groups are each independently optionally selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, -OH, -OR 2a , oxo, halogen, -C(O)R 2a , -C(O)OR 2a , -C(O)NR 2b R 2c , -CN, -NR 2b R 2c , 3-6-membered cycloalkyl, 3-7-membered heterocycloalkyl, 6-10-membered aryl substituted with a 5- to 10-membered heteroaryl group; the R 2a is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, 3-7 membered heterocycloalkyl, or -(CH 2 ) r OCH 3 , the r is 1, 2 or 3;
    所述R 2b为氢或C 1-C 6烷基； The R 2b is hydrogen or C 1 -C 6 alkyl;
    所述R 2c为氢或C 1-C 6烷基； The R 2c is hydrogen or C 1 -C 6 alkyl;
    R 2为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b,所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , the R a and R b are each independently hydrogen, C 1 -C 6 alkyl , C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 2为-NH-(CH 2) k-NH-C(O)-(C 1-C 6烷基)，所述k为1或者2； R 2 is -NH-(CH 2 ) k -NH-C(O)-(C 1 -C 6 alkyl), and the k is 1 or 2;
    R 2为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
    R 3和R 4各自独立的为氢、C 1-C 6烷基、C 1-C 6烷氧基或C 3-C 6环烷氧基；所述R 3和R 4至少有一个不为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基；所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代； R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy or C 3 -C 6 cycloalkoxy; at least one of said R 3 and R 4 is not hydrogen, or the R 3 and R 4 and the atoms to which they are attached together form a 3-6 membered cycloalkyl; the alkyl, alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy or halogen substituted;
    A为任选取代的6-元芳基或者任选取代的5-6元杂芳基；A is an optionally substituted 6-membered aryl or an optionally substituted 5-6 membered heteroaryl;
    Figure PCTCN2022088560-appb-100014
    Figure PCTCN2022088560-appb-100014
    其中所述S4中：Where the S4:
    Q 1为CH或者N； Q 1 is CH or N;
    Q 4为CH、C或者N； Q 4 is CH, C or N;
    每个Q 2各自独立的为C-R 1或者N，所述Q 2其中一个为N另一个Q 2为C-R 1； Each Q 2 is independently CR 1 or N, and one of the Q 2 is N and the other Q 2 is CR 1 ;
    每个Q 3和Q 5分子独立的为C(R QC) 2、NR QN、C(O)、O、S或者SO 2，所述R QC各自独立的为氢、F、Cl、Br、或者6-10元芳基，所述R QN各自独立的为氢、C 1-C 6烷基或者6-10元芳基； Each Q3 and Q5 molecule is independently C( RQC ) 2 , NRQN , C(O), O, S, or SO2, and each RQC is independently hydrogen , F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
    所述Q 1、Q 2、Q 3、Q 4、和Q 5至少有一个是N、NR QN、O或者SO 2； At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
    m为0、1、2或者3；m is 0, 1, 2 or 3;
    n为0、1、2或者3；n is 0, 1, 2 or 3;
    且当m为0时，n不是0；And when m is 0, n is not 0;
    R 1选自氢、C 1-C 6烷基、卤素、-C(O)NHR 1a、-NHR 1a、-OR 1a、环丙基、氮杂环丁烷或者-CN；所述C 1-C 6烷基和氮杂环丁烷任选的被选自卤素、R 1a、-NHR 1a或-OR 1a的取代基取代；所述R 1a为氢、C 1-C 6烷基、环丙基、3-6元杂环或者C 1-C 6卤代烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -C(O)NHR 1a , -NHR 1a , -OR 1a , cyclopropyl, azetidine or -CN; the C 1 - C6 alkyl and azetidine are optionally substituted with substituents selected from halogen, R 1a , -NHR 1a or -OR 1a ; said R 1a is hydrogen, C 1 -C 6 alkyl, cyclopropyl base, 3-6 membered heterocycle or C 1 -C 6 haloalkyl;
    L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-S(O)-、-S(＝O)(＝NH)-、-S(＝O)[＝N(C 1-C 6烷基)]-、-N(C 1-C 6烷基)-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -S(O)-, - S(=O)(=NH)-, -S(=O)[=N(C 1 -C 6 alkyl)]-, -N(C 1 -C 6 alkyl)-, -C(O) (CH 2 ) p -, -(CH 2 ) p - or O; the o is 0, 1 or 2; the p is an integer from 1 to 6;
    R 2选自氢、C 1-C 6烷基、-NR 2bR 2c、-OR 2a、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述C 1-C 6烷基、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基、C 1-C 6甲氧基烷基、-OH、-OR 2a、氧代基、卤素、＝N、-C(O)R 2a、-C(O)OR 2a、-C(O)NR 2bR 2c、-S(O) 2R 2a、-CN、-NR 2bR 2c、3-6元环烷基、3-7元杂环烷基、6-10元芳基或5-10元杂芳基的取代基取代；所述R 2a为氢、C 1-C 6烷基、C 1-C 6卤代烷基、3-7元杂环烷基、或者-(CH 2) rOCH 3，所述r为1、2或者3； R 2 is selected from hydrogen, C 1 -C 6 alkyl, -NR 2b R 2c , -OR 2a , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6 -10-membered aryl, 5-10-membered heteroaryl; the C 1 -C 6 -membered alkyl, 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-membered -10-membered aryl and 5-10-membered heteroaryl are each independently optionally selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 hydroxyalkyl, C 1 - C 6methoxyalkyl , -OH, -OR 2a , oxo, halogen, =N, -C(O)R 2a , -C(O)OR 2a , -C(O)NR 2b R 2c , -S(O) 2 R 2a , -CN, -NR 2b R 2c , 3-6 membered cycloalkyl, 3-7 membered heterocycloalkyl, 6-10 membered aryl or 5-10 membered heteroaryl Substituent substitution; the R 2a is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, 3-7 membered heterocycloalkyl, or -(CH 2 ) r OCH 3 , and the r is 1, 2 or 3;
    所述R 2b为氢或C 1-C 6烷基； The R 2b is hydrogen or C 1 -C 6 alkyl;
    所述R 2c为氢或C 1-C 6烷基； The R 2c is hydrogen or C 1 -C 6 alkyl;
    R 3和R 4各自独立的为氢、任选被卤素、-OH取代的C 1-C 6烷基，所述R 3和R 4至少有一个为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen, C 1 -C 6 alkyl optionally substituted by halogen, -OH, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and The atoms to which it is attached together form a 3-6 membered cycloalkyl;
    A为任选取代的6-元芳基或者任选取代的5-6元杂芳基；A is an optionally substituted 6-membered aryl or an optionally substituted 5-6 membered heteroaryl;
    条件是当
    Figure PCTCN2022088560-appb-100015
    为
    Figure PCTCN2022088560-appb-100016
    Figure PCTCN2022088560-appb-100017
    Figure PCTCN2022088560-appb-100018
    或者
    Figure PCTCN2022088560-appb-100019
    时，R 1不为氢；     condition is when
    Figure PCTCN2022088560-appb-100015
    for
    Figure PCTCN2022088560-appb-100016
    Figure PCTCN2022088560-appb-100017
    Figure PCTCN2022088560-appb-100018
    or
    Figure PCTCN2022088560-appb-100019
    , R 1 is not hydrogen;
    Figure PCTCN2022088560-appb-100020
    Figure PCTCN2022088560-appb-100020
    其中所述S5、S5'中：Wherein said S5, S5' in:
    所述R 1为氢或R a1； The R 1 is hydrogen or R a1 ;
    R a1选自C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 1-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10元芳基或者5-10元杂芳基，所述C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 1-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10元芳基和5-10元杂芳基任选的被1个或多个相同的或者不同的R b1和/或R c1取代； R a1 is selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 Cycloalkenyl, 3-10-membered heterocycloalkyl, C 6 -C 10 -membered aryl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 membered aryl and 5-10 membered heteroaryl is optionally substituted with one or more identical or different R b1 and/or R c1 ;
    每个R b1各自独立的为-OR c1、-NR c1R c1、卤素、-CN、-C(O)R c1、-C(O)OR c1、-C(O)NR c1R c1、-S(O) 2R c1、-S(O) 2NR c1R c1、-NHC(O)R c1、-N(C 1-C 4烷基)C(O)R c1、-NHC(O)OR c1或者-N(C 1-C 4烷基)C(O)OR c1； Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4alkyl )C(O)R c1 , -NHC(O) OR c1 or -N(C 1 -C 4 alkyl)C(O)OR c1 ;
    每个R c1各自独立的为氢、C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基或者5-10元杂芳基；所述C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基和5-10元杂芳基各自独立的任选的被1个或者多个相同的或者不同的R d1和/或R e1； Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl; the C 1 -C 6 alkyl, C 1 -C 6 Haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C The 10 -aryl and 5-10-membered heteroaryl groups are each independently optionally surrounded by 1 or more identical or different R d1 and/or R e1 ;
    每个R d1各自的独立为-OR e1、-NR e1R e1、卤素、-CN、-C(O)R e1、-C(O)OR e1、-C(O)NR e1R e1、-S(O)2R e1、-S(O) 2NR e1R e1、-NHC(O)R e1、-N(C 1-C 4烷基)C(O)R e1、-NHC(O)OR e1或者-N(C 1-C 4烷基)C(O)OR e1； Each R d1 is independently -OR e1 , -NR e1 R e1 , halogen, -CN, -C(O)R e1 , -C(O)OR e1 , -C(O)NR e1 R e1 , - S(O)2R e1 , -S(O) 2 NR e1 R e1 , -NHC(O)R e1 , -N(C 1 -C 4 alkyl)C(O)R e1 , -NHC(O)OR e1 or -N(C 1 -C 4 alkyl)C(O)OR e1 ;
    每个R e1各自独立的为氢、C 1-C 6烷基、C 1-C 6卤代烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 4-C 10环烯基、3-10元杂环烷基、C 6-C 10芳基或者5-10元杂芳基； Each R e1 is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 4 -C 10 cycloalkenyl, 3-10 membered heterocycloalkyl, C 6 -C 10 aryl or 5-10 membered heteroaryl;
    R 2选自氢、C 1-C 4烷基、C 3-C 6环烷基、3-6元杂环烷基或者卤素； R 2 is selected from hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl or halogen;
    环A选自C 6-C 10芳基、5-10元杂芳基或者9-10元双杂环烷基； Ring A is selected from C 6 -C 10 aryl, 5-10 membered heteroaryl or 9-10 membered biheterocycloalkyl;
    p为1、2或3；p is 1, 2 or 3;
    每个R 4各自独立的为氢、羟基、氧代、卤素、氰基、C 1-C 4烷基、-NH 2、C 1-C 4卤代烷基、C 2-C 4烯基、C 2-C 4炔基、C 1-C 4羟基烷基、羟基-C 1-C 4卤代烷基、C 3-C 6环烷基、C 3-C 6环烷氧基、3-6元杂环烷基、C 3-C 6羟基环烷基，被3-6元杂环烷基取代的C 1-C 4卤代烷基，被羟基、卤素、-NH 2、-S(O) 2-(C 1-C 4烷基)或者氧代基取代的3-6元杂环烷基，且氧代基仅在非芳香环上取代； Each R 4 is independently hydrogen, hydroxy, oxo, halogen, cyano, C 1 -C 4 alkyl, -NH 2 , C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkoxy, 3-6 membered heterocycle Alkyl, C 3 -C 6 hydroxycycloalkyl, C 1 -C 4 haloalkyl substituted by 3-6 membered heterocycloalkyl, substituted by hydroxy, halogen, -NH 2 , -S(O) 2 -(C 1 -C 4 alkyl) or oxo-substituted 3-6 membered heterocycloalkyl, and the oxo group is only substituted on a non-aromatic ring;
    R 4为-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 4 is -NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 4为-C(O)NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 4 is -C(O)NR a R b, and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 ring alkyl;
    R 4为-C(O)OR g，所述R g为氢或C 1-C 6烷基； R 4 is -C(O)OR g , and said R g is hydrogen or C 1 -C 6 alkyl;
    R 4为-OR h；所述R h为C 1-C 6烷基； R 4 is -OR h ; Described R h is C 1 -C 6 alkyl;
    或者，R 4为-(CH 2)NR aR b，所述R a和R b各自独立的氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； Alternatively, R 4 is -(CH 2 )NR a R b , and said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl, or C 3 -C 8 cycloalkyl;
    R 3和R 5各自独立的为氢、C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代。 R 3 and R 5 are each independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkane radical, alkoxy, cycloalkyl and cycloalkoxy optionally by cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen substituted.
  3. 如权利要求1或2所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述S为S1a、S1a'、-X-S1a'、S1a”、-X-S1a”、S2a、S2a'、-X-S2a'、S2a”、-X-S2a”、S3a、S4a、S5a、S5a'或-X-S5a'：X为O、NH或S，优选为O；The compound of formula I as claimed in claim 1 or 2, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or Its pharmaceutically acceptable salt, the S is S1a, S1a', -X-S1a', S1a", -X-S1a", S2a, S2a', -X-S2a', S2a", -X-S2a ", S3a, S4a, S5a, S5a' or -X-S5a': X is O, NH or S, preferably O;
    Figure PCTCN2022088560-appb-100021
    Figure PCTCN2022088560-appb-100021
    其中所述S1a、S1a'、S1a”中：Wherein said S1a, S1a', S1a":
    R 1选自氢、-OCH 3、-OCH 2CH 3、
    Figure PCTCN2022088560-appb-100022
    -CH 2OH、-C(O)OH、-C(O)OCH 3、-Br、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2、-O(CH 2) 3CH 3、-O(CH 2) 2OCH 3、
    Figure PCTCN2022088560-appb-100023
    -O(CH 2)-苯基、-N＝S(O)(CH 3) 2、-CH 3、环丙基、-N(CH 3) 2、-NHCH 3、-NH 2、
    Figure PCTCN2022088560-appb-100024
    Figure PCTCN2022088560-appb-100025
    -C(CH 3) 2-OH、
    Figure PCTCN2022088560-appb-100026
    -NH(CH 2)-NH-C(O)CH 3、-NH(CH 2)-吗啡啉、-NH-C(O)CH 3、-NH-C(O)NHCH 3、-NH-C(O)-N(CH 3) 2、硝基、-NH-S(O) 2CH 3、-N＝S(O)(CH 3) 2、羟基、-O-(CH 2) 2-S(O) 2CH 3、-F、
    Figure PCTCN2022088560-appb-100027
    Figure PCTCN2022088560-appb-100028
    Figure PCTCN2022088560-appb-100029
    环丙氧基、环丁氧基、环戊氧基、环己氧基、氮杂环丁烷基、氮杂环戊烷基、哌啶基、哌嗪基、氧杂环丁烷、氧杂环戊烷基、氧杂环己烷基、硫杂环丁烷基、硫杂环戊烷基、硫杂环己烷基、氮杂环丁烷氧基、氮杂环戊烷氧基、哌啶基氧基、哌嗪基氧基、氧杂环丁烷氧基、氧杂环戊烷氧基、氧杂环己烷氧基、硫杂环丁烷氧基、硫杂环戊烷氧基、硫杂环己烷氧基、     R 1 is selected from hydrogen, -OCH 3 , -OCH 2 CH 3 ,
    Figure PCTCN2022088560-appb-100022
    -CH 2 OH, -C(O)OH, -C(O)OCH 3 , -Br, -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 , -O(CH 2 ) 3 CH 3 , -O(CH 2 ) 2 OCH 3 ,
    Figure PCTCN2022088560-appb-100023
    -O(CH 2 )-phenyl, -N=S(O)(CH 3 ) 2 , -CH 3 , cyclopropyl, -N(CH 3 ) 2 , -NHCH 3 , -NH 2 ,
    Figure PCTCN2022088560-appb-100024
    Figure PCTCN2022088560-appb-100025
    -C(CH 3 ) 2 -OH,
    Figure PCTCN2022088560-appb-100026
    -NH(CH 2 )-NH-C(O)CH 3 , -NH(CH 2 )-morpholine, -NH-C(O)CH 3 , -NH-C(O)NHCH 3 , -NH-C (O)-N(CH 3 ) 2 , nitro, -NH-S(O) 2 CH 3 , -N=S(O)(CH 3 ) 2 , hydroxyl, -O-(CH 2 ) 2 -S (O) 2 CH 3 , -F,
    Figure PCTCN2022088560-appb-100027
    Figure PCTCN2022088560-appb-100028
    Figure PCTCN2022088560-appb-100029
    Cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy, azetidinyl, azetidinyl, piperidinyl, piperazinyl, oxetane, oxa Cyclopentyl, oxanyl, thietanyl, thietanyl, thietanyl, azetidinyloxy, azepanyloxy, piperidine Peridyloxy, piperazinyloxy, oxetanyloxy, oxolaneoxy, oxaneoxy, thietanyloxy, thietanyloxy , thianeoxy,
    Figure PCTCN2022088560-appb-100030
    Figure PCTCN2022088560-appb-100031
    -OCH 2CH 2CH 3、-OCH 2CH 2CH 2N(CH 3) 2、-OCH 2CH 2CH 2OH、
    Figure PCTCN2022088560-appb-100032
    Figure PCTCN2022088560-appb-100033
    -OCH 2CH 2NC(O)CH 3、-OCH 2CH 2N(CH 3) 2、-OCH 2CH 2OH、
    Figure PCTCN2022088560-appb-100034
    Figure PCTCN2022088560-appb-100035
    -SCH 3、-N(CH 3) 2、
    Figure PCTCN2022088560-appb-100036
    Figure PCTCN2022088560-appb-100030
    Figure PCTCN2022088560-appb-100031
    -OCH 2 CH 2 CH 3 , -OCH 2 CH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 CH 2 OH,
    Figure PCTCN2022088560-appb-100032
    Figure PCTCN2022088560-appb-100033
    -OCH 2 CH 2 NC(O)CH 3 , -OCH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 OH,
    Figure PCTCN2022088560-appb-100034
    Figure PCTCN2022088560-appb-100035
    -SCH 3 , -N(CH 3 ) 2 ,
    Figure PCTCN2022088560-appb-100036
    x为1或者2；x is 1 or 2;
    A 1选自
    Figure PCTCN2022088560-appb-100037
    Figure PCTCN2022088560-appb-100038
    A 1 is selected from
    Figure PCTCN2022088560-appb-100037
    Figure PCTCN2022088560-appb-100038
    R 2选自：氢、羟基、氧代基、氰基、环丙基、1，1-二甲基环丙基、-C(＝CH 2)CH 3、-C(CH 3)(＝CH 2)CH 3、-CH＝CH(CH 2) 2CH 3、-CH＝CHCH 3、-CH＝CH-环丙基、-C(O)NH 2、-C(O)OCH 3、-S(O) 2CH 3、-OCH 3、-CH 2NH 2、 三氟甲基、甲基、三氟甲氧基、卤素(F、Cl、Br)、-NH 2、-NHC(O)CH 3、-NHCH 2CH 3或-NHCH(CH 3) 2； R 2 is selected from: hydrogen, hydroxyl, oxo, cyano, cyclopropyl, 1,1-dimethylcyclopropyl, -C(=CH 2 )CH 3 , -C(CH 3 )(=CH 2 ) CH 3 , -CH=CH(CH 2 ) 2 CH 3 , -CH=CHCH 3 , -CH=CH-cyclopropyl, -C(O)NH 2 , -C(O)OCH 3 , -S (O) 2 CH 3 , -OCH 3 , -CH 2 NH 2 , trifluoromethyl, methyl, trifluoromethoxy, halogen (F, Cl, Br), -NH 2 , -NHC(O)CH 3. -NHCH 2 CH 3 or -NHCH(CH 3 ) 2 ;
    w为1、2或者3；w is 1, 2 or 3;
    A 2选自
    Figure PCTCN2022088560-appb-100039
    Figure PCTCN2022088560-appb-100040
    A 2 selected from
    Figure PCTCN2022088560-appb-100039
    Figure PCTCN2022088560-appb-100040
    R 3选自-C(O)NH(CH 2) 2CH 3、-C(O)N(CH 3) 2、-C(O)NH 2、-C(O)NH(CH 2) 2N(CH 3) 2、-CH 2C(O)NH 2、氢、-F、-Cl、-Br、氰基、-CF 3、-CH 3、-CH 2CH 3、-CH＝CH 2、-CH 2CN、-CH(CH 3)-NH 2、-CH＝CH-CN、-C(O)-OH、-C(O)OCH 3、-C(O)CH 3、-C(CH 3) 2-C(O)-OCH 3、-C(CH 3) 2-CN、氧代基、羟基、环丙基、环丁基、环戊基、-NH 2、-NH-C(O)CH 3、-NH-S(O) 2CH 3、-NH-C(O)OC(CH 3) 3、
    Figure PCTCN2022088560-appb-100041
    Figure PCTCN2022088560-appb-100042
    -S(O) 2CH 3、-S(O) 2NCH 3、-S(O) 2NH 2、-OCH 2CH 3、-O(CH 2) 2CH 3、-OCF 3、
    Figure PCTCN2022088560-appb-100043
    -OCH 2环丙基、-OCH 3、-O(CH 2) 3CH 3、-OCH 2苯基、-O-苯基、-(CH 2)-OH、-(CH 2) 2-OH、-(CH 2)-OCH 3、-(CH 2)-OCH 2CH 3、-CH(OH)-CH 2-苯基、-CH(OH)-CH 2CH 3、-CH(OH)-CH 2CH 2CH 3、-CH(OH)-CH 2CH 2CH 2CH 3、-CH(OH)-CH(CH 3) 2、-CH(OH)-苯基、-CH(OH)-CN、-CH(OH)-CH 2-OH、-CH(OH)-CF 3、-CH(OH)-(CH 2) 2-苯基、 ＊-CH（OH）-C≡CH、-CH(NH 2)-CH 2-C(O)OH、-CH 2-NH-S(O) 2-CH 3、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2、-CH 2-NH-CH 2CH 3、-CH(CH 3)-NH 2、-CH 2-NH 2、-CH 2CH 2-NH 2、-CH 2NH-CH 2-苯基、-CH 2N(CH 2CH 3) 2、-CH 2NH-环丙基、-CH 2NH-环丁基、-CH 2NH-环戊基、-CH 2NH-吡啶基、-CH 2NH-苯基、-CH 2NH-(CH 2) 2-OH、-CH 2N(CH 3)-(CH 2) 2-OH、-CH 2NH-CH 2-CN、-CH 2N(CH 3)-CH 2-CN、-CH 2N(CH 3)-CH 2-CF 3、-CH 2N(CH 3)-CH 2-CF 2H、-CH 2NH-CH 2-CF 2H、-CH 2NH-(CH 2) 2-OCH 3、
    Figure PCTCN2022088560-appb-100044
    Figure PCTCN2022088560-appb-100045
     R3 is selected from -C(O)NH( CH2 ) 2CH3 , -C(O)N( CH3 ) 2 , -C(O) NH2 , -C (O)NH( CH2 ) 2N (CH 3 ) 2 , -CH 2 C(O)NH 2 , hydrogen, -F, -Cl, -Br, cyano, -CF 3 , -CH 3 , -CH 2 CH 3 , -CH=CH 2 , -CH 2 CN, -CH(CH 3 )-NH 2 , -CH=CH-CN, -C(O)-OH, -C(O)OCH 3 , -C(O)CH 3 , -C(CH 3 ) 2 -C(O)-OCH 3 , -C(CH 3 ) 2 -CN, oxo, hydroxyl, cyclopropyl, cyclobutyl, cyclopentyl, -NH 2 , -NH-C(O )CH 3 , -NH-S(O) 2 CH 3 , -NH-C(O)OC(CH 3 ) 3 ,
    Figure PCTCN2022088560-appb-100041
    Figure PCTCN2022088560-appb-100042
    -S(O) 2 CH 3 , -S(O) 2 NCH 3 , -S(O) 2 NH 2 , -OCH 2 CH 3 , -O(CH 2 ) 2 CH 3 , -OCF 3 ,
    Figure PCTCN2022088560-appb-100043
    -OCH 2 cyclopropyl, -OCH 3 , -O(CH 2 ) 3 CH 3 , -OCH 2 phenyl, -O-phenyl, -(CH 2 )-OH, -(CH 2 ) 2 -OH, -(CH 2 )-OCH 3 , -(CH 2 )-OCH 2 CH 3 , -CH(OH)-CH 2 -phenyl, -CH(OH)-CH 2 CH 3 , -CH(OH)-CH 2CH2CH3 , -CH(OH ) -CH2CH2CH2CH3 , -CH(OH ) -CH ( CH3 ) 2 , -CH(OH ) -phenyl, -CH(OH)-CN , -CH(OH)-CH 2 -OH, -CH(OH)-CF 3 , -CH(OH)-(CH 2 ) 2 -phenyl, * -CH(OH)-C≡CH, -CH( NH 2 )-CH 2 -C(O)OH, -CH 2 -NH-S(O) 2 -CH 3 , -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 , -CH 2 -NH-CH 2 CH 3 , -CH(CH 3 )-NH 2 , -CH 2 -NH 2 , -CH 2 CH 2 -NH 2 , - CH2NH - CH2 -phenyl, -CH2N(CH2CH3)2 , -CH2NH - cyclopropyl , -CH2NH - cyclobutyl, -CH2NH - cyclopentyl, - CH2NH -pyridyl, -CH2NH-phenyl, -CH2NH-( CH2 ) 2 -OH, -CH2N ( CH3 )-( CH2 ) 2 - OH, -CH2NH- CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CF 3 , -CH 2 N(CH 3 )-CH 2 -CF 2 H, -CH 2 NH-CH 2 -CF 2 H, -CH 2 NH-(CH 2 ) 2 -OCH 3 ,
    Figure PCTCN2022088560-appb-100044
    Figure PCTCN2022088560-appb-100045
    Figure PCTCN2022088560-appb-100046
    Figure PCTCN2022088560-appb-100047
    -CH 2NH-C(O)-OC(CH 3) 3、-CH 2CH 2NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 2NOH、-CH 2NH-C(O)-CH 2OCH 3、-CH(CH 3)NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 3、
    Figure PCTCN2022088560-appb-100048
    -CH 2NHCH 2-C(O)-NH 2、-CH 2NHCH 2-C(O)-(CH 3) 2、-CH 2NHCH 2-C(O)-OCH 3、-CH 2NHCH 2-C(O)-NHCH 3、-CH 2NHCH 2-C(O)-NH(CH 2) 2-OCH 3、-CH 2NHCH 2-C(O)-NHCH 2-苯基、
    Figure PCTCN2022088560-appb-100049
    -CH 2NHCH 2-C(O)-NH-苯基、
    Figure PCTCN2022088560-appb-100050
    -CH 2NH-C(O)-CH 2NH-苯基、
    Figure PCTCN2022088560-appb-100051
    或-CH 2NH-C(O)-CH 2NH-CH 2CF 3；
    Figure PCTCN2022088560-appb-100046
    Figure PCTCN2022088560-appb-100047
    -CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 2 NOH, -CH 2 NH-C(O)-CH 2 OCH 3 , -CH(CH 3 )NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 3 ,
    Figure PCTCN2022088560-appb-100048
    -CH 2 NHCH 2 -C(O)-NH 2 , -CH 2 NHCH 2 -C(O)-(CH 3 ) 2 , -CH 2 NHCH 2 -C(O)-OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 3 , -CH 2 NHCH 2 -C(O)-NH(CH 2 ) 2 -OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 2 -phenyl,
    Figure PCTCN2022088560-appb-100049
    -CH 2 NHCH 2 -C(O)-NH-phenyl,
    Figure PCTCN2022088560-appb-100050
    -CH 2 NH-C(O)-CH 2 NH-phenyl,
    Figure PCTCN2022088560-appb-100051
    or -CH 2 NH-C(O)-CH 2 NH-CH 2 CF 3 ;
    y为1或者2；y is 1 or 2;
    L'为键、-(CH 2) k-或者-O(CH 2) k-，所述k为1或者2，或者L'为-CH＝CH-(CH 2) n-,所述n为0、1或者2； L' is a bond, -(CH 2 ) k - or -O(CH 2 ) k -, the k is 1 or 2, or L' is -CH=CH-(CH 2 ) n -, the n is 0, 1 or 2;
    Figure PCTCN2022088560-appb-100052
    Figure PCTCN2022088560-appb-100052
    Figure PCTCN2022088560-appb-100053
    Figure PCTCN2022088560-appb-100053
    其中所述S2a、S2a'、S2a”中：Wherein said S2a, S2a', S2a" in:
    T和V都为N，或者T为C，V为N，或者T为N，V为C；Both T and V are N, or T is C and V is N, or T is N and V is C;
    R 1选自氢、-OCH 3、-OCH 2CH 3、
    Figure PCTCN2022088560-appb-100054
    -CH 2OH、-C(O)OH、-C(O)OCH 3、-Br、-OCH(CH 3) 2、-O(CH 2) 2CH(CH 3) 2、-O(CH 2) 3CH 3、-O(CH 2) 2OCH 3、
    Figure PCTCN2022088560-appb-100055
    -O(CH 2) z-苯基、-N＝S(O)(CH 3) 2、-CH 3、环丙基、-N(CH 3) 2、-NHCH 3、-NH 2、
    Figure PCTCN2022088560-appb-100056
    Figure PCTCN2022088560-appb-100057
    -C(CH 3) 2-OH、
    Figure PCTCN2022088560-appb-100058
    -NH(CH 2)-NH-C(O)CH 3、-NH(CH 2)-吗啡啉、-NH-C(O)CH 3、-NH-C(O)NHCH 3、-NH-C(O)-N(CH 3) 2、硝基、-NH-S(O) 2CH 3、-N＝S(O)(CH 3) 2、羟基、-O-(CH 2) 2-S(O) 2CH 3、-F、
    Figure PCTCN2022088560-appb-100059
    Figure PCTCN2022088560-appb-100060
    Figure PCTCN2022088560-appb-100061
    环丙氧基、环丁氧基、环戊氧基、环己氧基、氮杂环丁烷基、氮杂环戊烷基、哌啶基、哌嗪基、氧杂环丁烷、氧杂环戊烷基、氧杂环己烷基、硫杂环丁烷基、硫杂环戊烷基、硫杂环己烷基、氮杂环丁烷氧基、氮杂环戊烷氧基、哌啶基氧基、哌嗪基氧基、氧杂环丁烷氧基、氧杂环戊烷氧基、氧杂环己烷氧基、硫杂环丁烷氧基、硫杂环戊烷氧基、硫杂环己烷氧基、     R 1 is selected from hydrogen, -OCH 3 , -OCH 2 CH 3 ,
    Figure PCTCN2022088560-appb-100054
    -CH 2 OH, -C(O)OH, -C(O)OCH 3 , -Br, -OCH(CH 3 ) 2 , -O(CH 2 ) 2 CH(CH 3 ) 2 , -O(CH 2 ) 3 CH 3 , -O(CH 2 ) 2 OCH 3 ,
    Figure PCTCN2022088560-appb-100055
    -O(CH 2 ) z -phenyl, -N=S(O)(CH 3 ) 2 , -CH 3 , cyclopropyl, -N(CH 3 ) 2 , -NHCH 3 , -NH 2 ,
    Figure PCTCN2022088560-appb-100056
    Figure PCTCN2022088560-appb-100057
    -C(CH 3 ) 2 -OH,
    Figure PCTCN2022088560-appb-100058
    -NH(CH 2 )-NH-C(O)CH 3 , -NH(CH 2 )-morpholine, -NH-C(O)CH 3 , -NH-C(O)NHCH 3 , -NH-C (O)-N(CH 3 ) 2 , nitro, -NH-S(O) 2 CH 3 , -N=S(O)(CH 3 ) 2 , hydroxyl, -O-(CH 2 ) 2 -S (O) 2 CH 3 , -F,
    Figure PCTCN2022088560-appb-100059
    Figure PCTCN2022088560-appb-100060
    Figure PCTCN2022088560-appb-100061
    Cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy, azetidinyl, azetidinyl, piperidinyl, piperazinyl, oxetane, oxa Cyclopentyl, oxanyl, thietanyl, thietanyl, thietanyl, azetidinyloxy, azepanyloxy, piperidine Peridyloxy, piperazinyloxy, oxetanyloxy, oxolaneoxy, oxaneoxy, thietanyloxy, thietanyloxy , thianeoxy,
    Figure PCTCN2022088560-appb-100062
    Figure PCTCN2022088560-appb-100062
    Figure PCTCN2022088560-appb-100063
    Figure PCTCN2022088560-appb-100064
    -OCH 2CH 2CH 3、-OCH 2CH 2CH 2N(CH 3) 2、-OCH 2CH 2CH 2OH、
    Figure PCTCN2022088560-appb-100065
    Figure PCTCN2022088560-appb-100066
    -OCH 2CH 2NC(O)CH 3、-OCH 2CH 2N(CH 3) 2、-OCH 2CH 2OH、
    Figure PCTCN2022088560-appb-100067
    Figure PCTCN2022088560-appb-100068
    -SCH 3、-N(CH 3) 2、
    Figure PCTCN2022088560-appb-100069
    Figure PCTCN2022088560-appb-100063
    Figure PCTCN2022088560-appb-100064
    -OCH 2 CH 2 CH 3 , -OCH 2 CH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 CH 2 OH,
    Figure PCTCN2022088560-appb-100065
    Figure PCTCN2022088560-appb-100066
    -OCH 2 CH 2 NC(O)CH 3 , -OCH 2 CH 2 N(CH 3 ) 2 , -OCH 2 CH 2 OH,
    Figure PCTCN2022088560-appb-100067
    Figure PCTCN2022088560-appb-100068
    -SCH 3 , -N(CH 3 ) 2 ,
    Figure PCTCN2022088560-appb-100069
    z为1或者2；z is 1 or 2;
    x为1或者2；x is 1 or 2;
    A 1选自
    Figure PCTCN2022088560-appb-100070
    Figure PCTCN2022088560-appb-100071
    A 1 is selected from
    Figure PCTCN2022088560-appb-100070
    Figure PCTCN2022088560-appb-100071
    R 2选自：氢、羟基、氧代基、氰基、环丙基、1，1-二甲基环丙基、-C(＝CH 2)CH 3、-C(CH 3)(＝CH 2)CH 3、-CH＝CH(CH 2) 2CH 3、-CH＝CHCH 3、-CH＝CH-环丙基、-C(O)NH 2、三氟甲基、甲基、三氟甲氧基、-C(O)OCH 3、-S(O) 2CH 3、-OCH 3、-CH 2NH 2或卤素(F、Cl、Br)； R 2 is selected from: hydrogen, hydroxyl, oxo, cyano, cyclopropyl, 1,1-dimethylcyclopropyl, -C(=CH 2 )CH 3 , -C(CH 3 )(=CH 2 ) CH 3 , -CH=CH(CH 2 ) 2 CH 3 , -CH=CHCH 3 , -CH=CH-cyclopropyl, -C(O)NH 2 , trifluoromethyl, methyl, trifluoro Methoxy, -C(O) OCH3 , -S(O) 2CH3 , -OCH3 , -CH2NH2 or halogen ( F, Cl , Br);
    w为1、2或者3；w is 1, 2 or 3;
    A 2选自
    Figure PCTCN2022088560-appb-100072
    A 2 selected from
    Figure PCTCN2022088560-appb-100072
    Figure PCTCN2022088560-appb-100073
    Figure PCTCN2022088560-appb-100073
    R 3选自-C(O)NH(CH 2) 2CH 3、-C(O)N(CH 3) 2、-C(O)NH 2、-C(O)NH(CH 2) 2N(CH 3) 2、-CH 2C(O)NH 2、氢、-F、-Cl、-Br、氰基、-CF 3、-CH 3、-CH 2CH 3、-CH＝CH 2、-CH 2CN、-CH(CH 3)-NH 2、-CH＝CH-CN、-C(O)-OH、-C(O)OCH 3、-C(O)CH 3、-C(CH 3) 2-C(O)-OCH 3、-C(CH 3) 2-CN、氧代基、羟基、环丙基、环丁基、环戊基、-NH 2、-NH-C(O)CH 3、-NH-S(O) 2CH 3、-NH-C(O)OC(CH 3) 3、
    Figure PCTCN2022088560-appb-100074
    Figure PCTCN2022088560-appb-100075
    -S(O) 2CH 3、-S(O) 2NCH 3、-S(O) 2NH 2、-OCH 2CH 3、-O(CH 2) 2CH 3、-OCF 3、
    Figure PCTCN2022088560-appb-100076
    -OCH 2环丙基、-OCH 3、-O(CH 2) 3CH 3、-OCH 2苯基、-O-苯基、-(CH 2)-OH、-(CH 2) 2-OH、-(CH 2)-OCH 3、-(CH 2)-OCH 2CH 3、-CH(OH)-CH 2-苯基、-CH(OH)-CH 2CH 3、-CH(OH)-CH 2CH 2CH 3、-CH(OH)-CH 2CH 2CH 2CH 3、-CH(OH)-CH(CH 3) 2、-CH(OH)-苯基、-CH(OH)-CN、-CH(OH)-CH 2-OH、-CH(OH)-CF 3、-CH(OH)-(CH 2) 2-苯基、 ＊-CH（OH）-C≡CH、-CH(NH 2)-CH 2-C(O)OH、-CH 2-NH-S(O) 2-CH 3、-CH 2-NH-(CH 2) 3CH 3、-CH 2-NH-CH 3、-CH 2-N(CH 3) 2、-CH 2-NH-CH 2CH 3、-CH(CH 3)-NH 2、-CH 2-NH 2、-CH 2CH 2-NH 2、-CH 2NH-CH 2-苯基、-CH 2N(CH 2CH 3) 2、-CH 2NH-环丙基、-CH 2NH-环丁基、-CH 2NH-环戊基、-CH 2NH-吡啶基、-CH 2NH-苯基、-CH 2NH-(CH 2) 2-OH、-CH 2N(CH 3)-(CH 2) 2-OH、-CH 2NH-CH 2-CN、-CH 2N(CH 3)-CH 2-CN、-CH 2N(CH 3)-CH 2-CF 3、-CH 2N(CH 3)-CH 2-CF 2H、-CH 2NH-CH 2-CF 2H、-CH 2NH-(CH 2) 2-OCH 3、
    Figure PCTCN2022088560-appb-100077
    Figure PCTCN2022088560-appb-100078
    Figure PCTCN2022088560-appb-100079
    -CH 2NH-C(O)-OC(CH 3) 3、-CH 2CH 2NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 2NOH、-CH 2NH-C(O)-CH 2OCH 3、-CH(CH 3)NH-C(O)-OC(CH 3) 3、-CH 2NH-C(O)-CH 3、
    Figure PCTCN2022088560-appb-100080
    -CH 2NHCH 2-C(O)-NH 2、-CH 2NHCH 2-C(O)-(CH 3) 2、-CH 2NHCH 2-C(O)-OCH 3、-CH 2NHCH 2-C(O)-NHCH 3、-CH 2NHCH 2-C(O)-NH(CH 2) 2-OCH 3、-CH 2NHCH 2-C(O)-NHCH 2-苯基、
    Figure PCTCN2022088560-appb-100081
    -CH 2NHCH 2-C(O)-NH-苯基、
    Figure PCTCN2022088560-appb-100082
    -CH 2NH-C(O)-CH 2NH-苯基、
    Figure PCTCN2022088560-appb-100083
    或-CH 2NH-C(O)-CH 2NH-CH 2CF 3；     R3 is selected from -C(O)NH( CH2 ) 2CH3 , -C(O)N( CH3 ) 2 , -C(O) NH2 , -C (O)NH( CH2 ) 2N (CH 3 ) 2 , -CH 2 C(O)NH 2 , hydrogen, -F, -Cl, -Br, cyano, -CF 3 , -CH 3 , -CH 2 CH 3 , -CH=CH 2 , -CH 2 CN, -CH(CH 3 )-NH 2 , -CH=CH-CN, -C(O)-OH, -C(O)OCH 3 , -C(O)CH 3 , -C(CH 3 ) 2 -C(O)-OCH 3 , -C(CH 3 ) 2 -CN, oxo, hydroxyl, cyclopropyl, cyclobutyl, cyclopentyl, -NH 2 , -NH-C(O )CH 3 , -NH-S(O) 2 CH 3 , -NH-C(O)OC(CH 3 ) 3 ,
    Figure PCTCN2022088560-appb-100074
    Figure PCTCN2022088560-appb-100075
    -S(O) 2 CH 3 , -S(O) 2 NCH 3 , -S(O) 2 NH 2 , -OCH 2 CH 3 , -O(CH 2 ) 2 CH 3 , -OCF 3 ,
    Figure PCTCN2022088560-appb-100076
    -OCH 2 cyclopropyl, -OCH 3 , -O(CH 2 ) 3 CH 3 , -OCH 2 phenyl, -O-phenyl, -(CH 2 )-OH, -(CH 2 ) 2 -OH, -(CH 2 )-OCH 3 , -(CH 2 )-OCH 2 CH 3 , -CH(OH)-CH 2 -phenyl, -CH(OH)-CH 2 CH 3 , -CH(OH)-CH 2CH2CH3 , -CH(OH ) -CH2CH2CH2CH3 , -CH(OH ) -CH ( CH3 ) 2 , -CH(OH ) -phenyl, -CH(OH)-CN , -CH(OH)-CH 2 -OH, -CH(OH)-CF 3 , -CH(OH)-(CH 2 ) 2 -phenyl, * -CH(OH)-C≡CH, -CH( NH 2 )-CH 2 -C(O)OH, -CH 2 -NH-S(O) 2 -CH 3 , -CH 2 -NH-(CH 2 ) 3 CH 3 , -CH 2 -NH-CH 3 , -CH 2 -N(CH 3 ) 2 , -CH 2 -NH-CH 2 CH 3 , -CH(CH 3 )-NH 2 , -CH 2 -NH 2 , -CH 2 CH 2 -NH 2 , - CH2NH - CH2 -phenyl, -CH2N(CH2CH3)2 , -CH2NH - cyclopropyl , -CH2NH - cyclobutyl, -CH2NH - cyclopentyl, - CH2NH -pyridyl, -CH2NH-phenyl, -CH2NH-( CH2 ) 2 -OH, -CH2N ( CH3 )-( CH2 ) 2 - OH, -CH2NH- CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CN, -CH 2 N(CH 3 )-CH 2 -CF 3 , -CH 2 N(CH 3 )-CH 2 -CF 2 H, -CH 2 NH-CH 2 -CF 2 H, -CH 2 NH-(CH 2 ) 2 -OCH 3 ,
    Figure PCTCN2022088560-appb-100077
    Figure PCTCN2022088560-appb-100078
    Figure PCTCN2022088560-appb-100079
    -CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 CH 2 NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 2 NOH, -CH 2 NH-C(O)-CH 2 OCH 3 , -CH(CH 3 )NH-C(O)-OC(CH 3 ) 3 , -CH 2 NH-C(O)-CH 3 ,
    Figure PCTCN2022088560-appb-100080
    -CH 2 NHCH 2 -C(O)-NH 2 , -CH 2 NHCH 2 -C(O)-(CH 3 ) 2 , -CH 2 NHCH 2 -C(O)-OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 3 , -CH 2 NHCH 2 -C(O)-NH(CH 2 ) 2 -OCH 3 , -CH 2 NHCH 2 -C(O)-NHCH 2 -phenyl,
    Figure PCTCN2022088560-appb-100081
    -CH 2 NHCH 2 -C(O)-NH-phenyl,
    Figure PCTCN2022088560-appb-100082
    -CH 2 NH-C(O)-CH 2 NH-phenyl,
    Figure PCTCN2022088560-appb-100083
    or -CH 2 NH-C(O)-CH 2 NH-CH 2 CF 3 ;
    Y为1或者2；Y is 1 or 2;
    L'为键、-(CH 2)k-或者-O(CH 2) k-，所述k为1或者2，或者L'为-CH＝CH-(CH 2) n-,所述n为0或者1； L' is a bond, -(CH 2 ) k- or -O(CH 2 ) k -, the k is 1 or 2, or L' is -CH=CH-(CH 2 ) n -, the n is 0 or 1;
    Figure PCTCN2022088560-appb-100084
    Figure PCTCN2022088560-appb-100084
    其中所述S3a中：Where said S3a:
    Q 1和Q 2各自独立的CH或者N； Q 1 and Q 2 are each independent CH or N;
    Q 3和Q 4各自独立的为C或者N，所述Q 3和Q 4至少有一个为C； Q 3 and Q 4 are independently C or N, and at least one of the Q 3 and Q 4 is C;
    Q 6为CH、N、NH、O或者S； Q 6 is CH, N, NH, O or S;
    Q 5为CH、N、NH、O或者S； Q 5 is CH, N, NH, O or S;
    所述Q 1、Q 2、Q 3、Q 4、Q 5和Q 6中至少有一个为N、NH、O或者S； At least one of the Q 1 , Q 2 , Q 3 , Q 4 , Q 5 and Q 6 is N, NH, O or S;
    R 1选自氢、C 1-C 6烷基、卤素、-OR 1a、环丙基或者-CN；所述R 1a为氢或C 1-C 6烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, -OR 1a , cyclopropyl or -CN; said R 1a is hydrogen or C 1 -C 6 alkyl;
    L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
    R 2选自氢、-(CH 2) qCH 3、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述q为1至5的整数；所述3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基和5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、-OH、卤素、-C(O)R 2a、-C(O)NR 2bR 2c的取代基取代；所述R 2a为C 1-C 6烷基或者-(CH 2) rOCH 3，所述r为1、2或者3；所述R 2b为氢或C 1-C 6烷基；所述R 2c为氢或C 1-C 6烷基； R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; said q is an integer from 1 to 5; said 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl and 5 -10-membered heteroaryl groups are each independently optionally substituted with a substituent selected from C 1 -C 6 alkyl, -OH, halogen, -C(O)R 2a , -C(O)NR 2b R 2c ; The R 2a is C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 , the r is 1, 2 or 3; the R 2b is hydrogen or C 1 -C 6 alkyl; the R 2c is hydrogen or C 1 -C 6 alkyl;
    R 3和R 4各自独立的为氢或C 1-C 6烷基，所述R 3和R 4至少有一个不为氢，或者所述R 3和R 4和其所连 接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is not hydrogen, or said R 3 and R 4 together with the atoms to which they are attached form 3 -6-membered cycloalkyl;
    A为任选取代的苯基或者任选取代的5-6元杂芳基；A is optionally substituted phenyl or optionally substituted 5-6 membered heteroaryl;
    Figure PCTCN2022088560-appb-100085
    Figure PCTCN2022088560-appb-100085
    其中所述S4a中：Where said S4a:
    Q 1为CH或者N； Q 1 is CH or N;
    Q 4为CH、C或者N； Q 4 is CH, C or N;
    每个Q 2各自独立的为CR 1或者N； Each Q 2 is independently CR 1 or N;
    每个Q 3和Q 5分子独立的为C(R QC) 2、NR QN、C(O)、O、S或者SO 2，所述R QC各自独立的为氢、F、Cl、Br、或者6-10元芳基，所述R QN各自独立的为氢、C 1-C 6烷基或者6-10元芳基； Each Q3 and Q5 molecule is independently C( RQC ) 2 , NRQN , C(O), O, S, or SO2, and each RQC is independently hydrogen , F, Cl, Br, or 6-10-membered aryl, each of the R QNs is independently hydrogen, C 1 -C 6 alkyl or 6-10-membered aryl;
    所述Q 1、Q 2、Q 3、Q 4、和Q 5至少有一个是N、NR QN、O或者SO 2； At least one of said Q 1 , Q 2 , Q 3 , Q 4 , and Q 5 is N, NR QN , O or SO 2 ;
    R 1选自氢、C 1-C 6烷基、卤素、环丙基、氰基或-OR 1a，所述R 1a为氢或C 1-C 6烷基； R 1 is selected from hydrogen, C 1 -C 6 alkyl, halogen, cyclopropyl, cyano or -OR 1a , said R 1a is hydrogen or C 1 -C 6 alkyl;
    L 2选自键、-C(O)-、-C(O)O-、-C(O)NH(CH 2) o-、-S(O) 2-、-C(O)(CH 2) p-、-(CH 2) p-或者O；所述o为0、1或者2；所述p为1至6的整数； L 2 is selected from bond, -C(O)-, -C(O)O-, -C(O)NH(CH 2 ) o -, -S(O) 2 -, -C(O)(CH 2 ) p -, -(CH 2 ) p - or 0; the o is 0, 1 or 2; the p is an integer from 1 to 6;
    R 2选自氢、-(CH 2) qCH 3、3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基；所述q为1至5的倍数；所述3-14元环烷基、3-14元环烯基、3-14元杂环烷基、6-10元芳基、5-10元杂芳基各自独立的任选的被选自C 1-C 6烷基、羟基、卤素、-C(O)R 2a或-C(O)NR 2bR 2c的基团取代；所述R 2a选自C 1-C 6烷基或-(CH 2) rOCH 3；所述r为1、2或者3；所述R 2b和R 2c各自独立的为氢或C 1-C 6烷基； R 2 is selected from hydrogen, -(CH 2 ) q CH 3 , 3-14 membered cycloalkyl, 3-14 membered cycloalkenyl, 3-14 membered heterocycloalkyl, 6-10 membered aryl, 5-10 membered aryl membered heteroaryl; the q is a multiple of 1 to 5; the 3-14-membered cycloalkyl, 3-14-membered cycloalkenyl, 3-14-membered heterocycloalkyl, 6-10-membered aryl, 5-membered -10-membered heteroaryl groups are each independently optionally substituted with a group selected from C 1 -C 6 alkyl, hydroxy, halogen, -C(O)R 2a or -C(O)NR 2b R 2c ; the The R 2a is selected from C 1 -C 6 alkyl or -(CH 2 ) r OCH 3 ; the r is 1, 2 or 3; the R 2b and R 2c are each independently hydrogen or C 1 -C 6 alkyl;
    R 3和R 4各自独立的为氢或C 1-C 6烷基，所述R 3和R 4至少有一个为氢，或者所述R 3和R 4和其所连接的原子一起形成3-6元环烷基； R 3 and R 4 are each independently hydrogen or C 1 -C 6 alkyl, at least one of said R 3 and R 4 is hydrogen, or said R 3 and R 4 and the atoms to which they are attached together form a 3- 6-membered cycloalkyl;
    A为任选取代的6-元芳基或者任选取代的5-6元杂芳基；A is an optionally substituted 6-membered aryl or an optionally substituted 5-6 membered heteroaryl;
    Figure PCTCN2022088560-appb-100086
    Figure PCTCN2022088560-appb-100086
    其中，所述S5a、S5a'中，R 1、R 2、R 3、R 4、环A和p如权利要求2中的S5中所定义和描述。 Wherein, in said S5a, S5a', R 1 , R 2 , R 3 , R 4 , ring A and p are as defined and described in S5 in claim 2 .
  4. 如权利要求1所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述S为S6、S6'、-X-S6'、S6”、S6”'、-X-S6”'、S6a、S6a”、S6c、S6c”、-X-S6c或-X-S6c”，优选为S6c：其中，X为O、NH或S，优选为O；The compound of formula I as claimed in claim 1, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceuticals An acceptable salt above, the S is S6, S6', -X-S6', S6", S6"', -X-S6"', S6a, S6a", S6c, S6c", -X-S6c or -X-S6c", preferably S6c: wherein X is O, NH or S, preferably O;
    Figure PCTCN2022088560-appb-100087
    Figure PCTCN2022088560-appb-100087
    其中所述S6、S6'、S6”、S6”'、S6a、S6a”、S6c、S6c”中：Wherein the S6, S6', S6", S6"', S6a, S6a", S6c, S6c" are:
    R 2选自氢、卤素、-OH、-CN、-NO 2、C 1-C 6烷基巯基或-NR aR b，所述R a和R b各自独立的为氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is selected from hydrogen, halogen, -OH, -CN, -NO 2 , C 1 -C 6 alkylmercapto or -NR a R b , said R a and R b are each independently hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 2选自C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷氧基、C 3-C 6杂环烷氧基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、4-7元杂环烷基、5-10元杂环烯烃基、螺杂环烷基、稠杂环烷基、桥杂环烷基、苯基、杂芳基、C 1-C 6卤代烷基、-COOH、-COOR c；所述R c为-C 1-C 6烷基、C 3-C 6烯基、C 3-C 6炔基、C 3-C 8环烷基或-C 4-C 8环烯基； R 2 is selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkoxy, C 3 -C 6 heterocycloalkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 4-7 membered heterocycloalkyl, 5-10 membered heterocycloalkenyl, spiroheterocycloalkyl, Condensed heterocycloalkyl, bridged heterocycloalkyl, phenyl, heteroaryl, C 1 -C 6 haloalkyl, -COOH, -COOR c ; the R c is -C 1 -C 6 alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 8 cycloalkyl or -C 4 -C 8 cycloalkenyl;
    R 2为-NS(O)(R d)(R e)，所述R d和R e各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、C 4-C 8环烯基、6-10元芳基或5-10元杂芳基； R 2 is -NS(O)(R d )(R e ), and said R d and R e are each independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkyne base, C 3 -C 8 cycloalkyl, C 4 -C 8 cycloalkenyl, 6-10 membered aryl or 5-10 membered heteroaryl;
    R 2为-NHC(O)-(C 1-C 6烷基)、-NHC(O)-NR aR b，所述R a和R b各自独立的为氢、-C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； R 2 is -NHC(O)-(C 1 -C 6 alkyl), -NHC(O)-NR a R b , and said R a and R b are each independently hydrogen, -C 1 -C 6 alkane radical, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 2为-NH-(CH 2) k-NH-C(O)-R aa，所述R aa为C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基，且k为1或者2； R 2 is -NH-(CH 2 ) k -NH-C(O)-R aa which is C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl, and k is 1 or 2;
    R 2为-NH-(CH 2) i-R f，所述i为0，1或者2且R f为4-7元杂环烷基、杂芳基、C 1-C 6烷基磺酰基； R 2 is -NH-(CH 2 ) i -R f , wherein i is 0, 1 or 2 and R f is 4-7 membered heterocycloalkyl, heteroaryl, C 1 -C 6 alkylsulfonyl ;
    此外以上所述C 1-C 6烷基、C 1-C 6烷氧基、4-7元杂环烷基和杂芳基任选的被1个、2个或者3个选自卤素、-OH、氧代、-CN、-NO 2、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 8环烷基、4-7元杂环烷基、C 1-C 6烷氧基、C 1-C 6卤代烷基、C 1-C 6卤代烷氧基、C 1-C 6烷基磺酰基、苯基、苄基、杂芳基、-(CH 2)-杂芳基、-NHC(O)(C 1-C 6烷基)、C 3-C 8环烷氧基、苯氧基、杂芳基氧基或者-NR aR b的基团取代；所述R a和R b各自独立的选自氢、C 1-C 6烷基、C 3-C 8杂环烷基或C 3-C 8环烷基； In addition, the above-mentioned C 1 -C 6 alkyl, C 1 -C 6 alkoxy, 4-7 membered heterocycloalkyl and heteroaryl are optionally selected from halogen, - OH, oxo, -CN, -NO 2 , C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 8 cycloalkyl, 4-7 membered hetero Cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylsulfonyl, phenyl, benzyl, heteroaryl, -(CH 2 )-heteroaryl, -NHC(O)(C 1 -C 6 alkyl), C 3 -C 8 cycloalkoxy, phenoxy, heteroaryloxy or -NR a R b The group is substituted; the R a and R b are each independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 8 heterocycloalkyl or C 3 -C 8 cycloalkyl;
    R 2为-O-(CH 2) z-苯基、-O-(CH 2) z-(4-7元杂环烷基)、-O-(CH 2) z-杂芳基，所述z为0，1或2，所述苯基、杂环烷基和杂芳基任选的被选自-OH、杂环烷基或者杂环烯基取代，且能被甲基或者氧代基取代； R 2 is -O-(CH 2 ) z -phenyl, -O-(CH 2 ) z -(4-7 membered heterocycloalkyl), -O-(CH 2 ) z -heteroaryl, said z is 0, 1 or 2, the phenyl, heterocycloalkyl and heteroaryl groups are optionally substituted with -OH, heterocycloalkyl or heterocycloalkenyl, and can be methyl or oxo replace;
    或者R 2为 or R2 for
    Figure PCTCN2022088560-appb-100088
    Figure PCTCN2022088560-appb-100089
    或者
    Figure PCTCN2022088560-appb-100090
    Figure PCTCN2022088560-appb-100088
    Figure PCTCN2022088560-appb-100089
    or
    Figure PCTCN2022088560-appb-100090
    R 1为氢或-OR A； R 1 is hydrogen or -OR A ;
    R A为氢、C 3-C 10环烷基或3-10元杂环烷基；所述C 3-C 10环烷基和3-10元杂环烷基任选被1个或者多个相同或不同的R a1和/或R c1取代； R A is hydrogen, C 3 -C 10 cycloalkyl or 3-10 membered heterocycloalkyl; the C 3 -C 10 cycloalkyl and 3-10 membered heterocycloalkyl are optionally composed of one or more same or different R a1 and/or R c1 substitutions;
    每个R a1各自独立的为C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基；所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基各自独立的任选的被1个或者多个相同或不同的R b1和/或R c1取代； Each R a1 is independently C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3 -10-membered heterocycloalkyl or 5-10-membered heteroaryl; said C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl , C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are each independently optionally substituted by one or more identical or different R b1 and/or R c1 ;
    每个R b1各自独立的为-OR c1、-NR c1R c1、卤素、-CN、-C(O)R c1、-C(O)OR c1、-C(O)NR c1R c1、-S(O) 2R c1、-S(O) 2NR c1R c1、-NHC(O)R c1、-N(C 1-C 4烷基)C(O)R c1、氧代基所取代，且所述氧代基仅在非芳香环取代； Each R b1 is independently -OR c1 , -NR c1 R c1 , halogen, -CN, -C(O)R c1 , -C(O)OR c1 , -C(O)NR c1 R c1 , - S(O) 2 R c1 , -S(O) 2 NR c1 R c1 , -NHC(O)R c1 , -N(C 1 -C 4 alkyl)C(O)R c1 , oxo substituted , and the oxo group is only substituted on a non-aromatic ring;
    每个R c1各自独立的为氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10杂芳基； Each R c1 is independently hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl , 3-10 membered heterocycloalkyl or 5-10 heteroaryl;
    或者R 1选自C 3-C 10环烷基、C 3-C 10环烯基、C 6-C 10芳基、3-10元杂环烷基或5-10元杂芳基；所述C 3-C 10环烷基、C 3-C 10环烯基、C 6-C 10芳基、3-10元杂环烷基或5-10元杂芳基任选的被1个或多个R a2和/或R b2取代； or R 1 is selected from C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl; the C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkenyl, C 6 -C 10 aryl, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl are optionally surrounded by one or more R a2 and/or R b2 substitutions;
    每个R a2各自独立的选自C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R c2和/或R b2取代； Each R a2 is independently selected from C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkane base, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl optionally substituted by 1 or more R c2 and/or R b2 ;
    每个R b2各自独立的选自-OR c2、-NR c2R c2、卤素、-CN、-C(O)R c2、-C(O)OR c2、-C(O)NR c2R c2、-OC(O)R c2、-S(O) 2R c2、-S(O) 2NR c2R c2、-NHC(O)R c2、-N(C 1-C 4烷基)C(O)R c2、-NHC(O)OR c2、氧代基、＝NH，且所述氧代基、＝NH仅在非芳香环上取代； Each R b2 is independently selected from -OR c2 , -NR c2 R c2 , halogen, -CN, -C(O)R c2 , -C(O)OR c2 , -C(O)NR c2 R c2 , -OC(O)R c2 , -S(O) 2 R c2 , -S(O) 2 NR c2 R c2 , -NHC(O)R c2 , -N(C 1 -C 4 alkyl)C(O ) R c2 , -NHC(O)OR c2 , oxo, =NH, and said oxo, =NH are only substituted on non-aromatic rings;
    每个R c2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、 3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R d2和/或R e2取代； Each R c2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d2 and/or R e2 ;
    每个R d2各自独立的为-OR e2、-NR e2R e2、卤素、-CN、-C(O)R e2、-C(O)OR e2、-C(O)NR e2R e2、-S(O) 2R e2、-S(O) 2NR e2R e2、-NHC(O)R e2、-N(C 1-C 4烷基)C(O)R e2、氧代基，所述氧代基仅在非芳香环上取代； Each R d2 is independently -OR e2 , -NR e2 Re2 , halogen, -CN, -C(O)R e2 , -C(O)OR e2 , -C(O)NR e2 Re2 , - S(O) 2 R e2 , -S(O) 2 NR e2 R e2 , -NHC(O)R e2 , -N(C 1 -C 4 alkyl)C(O)R e2 , oxo, all The oxo group is only substituted on a non-aromatic ring;
    每个R e2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R f2和/或R g2取代； Each R e2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R f2 and/or R g2 ;
    每个R f2各自独立的选自-OR g2、-NR g2R g2、卤素、-CN、-C(O)R g2、-C(O)OR g2、-C(O)NR g2R g2、-S(O) 2R g2、-S(O) 2NR g2R g2、-NHC(O)R g2、-N(C 1-C 4烷基)C(O)R g2、氧代基，所述氧代基仅在非芳香环上取代； Each R f2 is independently selected from -OR g2 , -NR g2 R g2 , halogen, -CN, -C(O)R g2 , -C(O)OR g2 , -C(O)NR g2 R g2 , -S(O) 2 R g2 , -S(O) 2 NR g2 R g2 , -NHC(O)R g2 , -N(C 1 -C 4 alkyl)C(O)R g2 , oxo, The oxo group is only substituted on a non-aromatic ring;
    每个R g2各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基； Each R g2 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
    或R 1选自C 2-C 4烷基、C 2-C 4烯基；所述C 2-C 4烷基和C 2-C 4烯基任选的R b3取代； or R 1 is selected from C 2 -C 4 alkyl, C 2 -C 4 alkenyl; the C 2 -C 4 alkyl and C 2 -C 4 alkenyl are optionally substituted by R b3 ;
    R b3选自-C(O)R c3、-C(O)OR c3、-C(O)NR  c3R c3、-C(O)NHOR c3或者-C(O)N(C 1-C 4烷基)OR c3； R b3 is selected from -C(O)R c3 , -C(O)OR c3 , -C(O)NR c3 R c3 , -C(O)NHOR c3 or -C(O)N(C 1 -C 4 alkyl) OR c3 ;
    每个R c3各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基，所述C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基任选被1个或者多个R d3和/或R e3取代； Each R c3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl, the C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 Cycloalkyl, C 6 -C 10 aryl, 3-10-membered heterocycloalkyl or 5-10-membered heteroaryl are optionally substituted by one or more R d3 and/or R e3 ;
    每个R d3各自独立的选自-OR e3、-NR e3R e3、卤素、-CN、-C(O)R e3、-C(O)OR e3、-C(O)NR e3R e3、-S(O) 2R e3、-S(O) 2NR e3R e3、-NHC(O)R e3、-N(C 1-C 4烷基)C(O)R e3、氧代基，所述氧代基仅在非芳香环上取代； Each R d3 is independently selected from -OR e3 , -NR e3 R e3 , halogen, -CN, -C(O)R e3 , -C(O)OR e3 , -C(O)NR e3 R e3 , -S(O) 2 R e3 , -S(O) 2 NR e3 R e3 , -NHC(O)R e3 , -N(C 1 -C 4 alkyl)C(O)R e3 , oxo, The oxo group is only substituted on a non-aromatic ring;
    每个R e3各自独立的选自氢、C 1-C 6烷基、C 2-C 6烯基、C 2-C 6炔基、C 3-C 10环烷基、C 6-C 10芳基、3-10元杂环烷基或者5-10元杂芳基； Each R e3 is independently selected from hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl base, 3-10 membered heterocycloalkyl or 5-10 membered heteroaryl;
    R 3选自氢、C 1-C 4烷基、-O(C 1-C 4烷基)、-NH 2、-NH(C 1-C 4烷基)、-N(C 1-C 4烷基) 2或者卤素； R 3 is selected from hydrogen, C 1 -C 4 alkyl, -O(C 1 -C 4 alkyl), -NH 2 , -NH(C 1 -C 4 alkyl), -N(C 1 -C 4 alkyl) 2 or halogen;
    R 5选自氢、羟基或者-NHR’； R 5 is selected from hydrogen, hydroxyl or -NHR';
    R’选自氢、C 1-C 3烷基和-C(O)C 1-C 3烷基； R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
    R 4选自C 1-C 4烷基、羟基、氧代、氰基、C 1-C 4烷氧基、C 1-C 4卤代烷基、C 1-C 4羟基烷基、羟基-C 1-C 4卤代烷基、C 2-C 6烯基、-C 2-C 6炔基、C 3-C 6环烷氧基、C 3-C 6环烷基、3-6元杂环烷基、3-6元羟基杂环烷基、卤素或者-SO 2-C 1-C 4烷基； R 4 is selected from C 1 -C 4 alkyl, hydroxy, oxo, cyano, C 1 -C 4 alkoxy, C 1 -C 4 haloalkyl, C 1 -C 4 hydroxyalkyl, hydroxy-C 1 -C 4 haloalkyl, C 2 -C 6 alkenyl, -C 2 -C 6 alkynyl, C 3 -C 6 cycloalkoxy, C 3 -C 6 cycloalkyl, 3-6 membered heterocycloalkyl , 3-6 membered hydroxy heterocycloalkyl, halogen or -SO 2 -C 1 -C 4 alkyl;
    R 6选自氢、C 1-C 4烷基或者卤素； R 6 is selected from hydrogen, C 1 -C 4 alkyl or halogen;
    或者R 4、R 6与它们连接的碳原子一起形成任选取代的C 5-C 6环烷基和5-6元杂环烷基，所述5-6元杂环烷基中的杂原子选自包含1、2、3或4个独立选自-NH、-O-、-S-和N的杂原子或杂原子团； Or R 4 , R 6 together with the carbon atom to which they are attached form optionally substituted C 5 -C 6 cycloalkyl and 5-6 membered heterocycloalkyl, the heteroatom in said 5-6 membered heterocycloalkyl is selected from a heteroatom or group of heteroatoms comprising 1, 2, 3 or 4 independently selected from -NH, -O-, -S- and N;
    R 7、R 8各自独立的为C 1-C 6烷基、C 1-C 6烷氧基、C 3-C 6环烷基或C 3-C 6环烷氧基，所述烷基、烷氧基、环烷基和环烷氧基任选的被氰基、羟基、C 1-C 6烷氧基、C 3-C 6环烷基、C 3-C 6环烷氧基或卤素取代。 R 7 and R 8 are each independently C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 3 -C 6 cycloalkyl or C 3 -C 6 cycloalkoxy, the alkyl, Alkoxy, cycloalkyl and cycloalkoxy are optionally cyano, hydroxy, C1 - C6alkoxy , C3 - C6cycloalkyl, C3 - C6cycloalkoxy or halogen replace.
  5. 如权利要求4所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中，R 1为氢或-OR A； The compound of formula I as claimed in claim 4, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceuticals thereof An acceptable salt of the above, wherein R 1 is hydrogen or -OR A ;
    R A为氢； R A is hydrogen;
    R 2为氢、C 1-C 4烷基或者-O(C 1-C 4烷基)，所述-O(C 1-C 4烷基)任选的被-O(C 1-C 4烷基)取代； R 2 is hydrogen, C 1 -C 4 alkyl or -O(C 1 -C 4 alkyl), said -O(C 1 -C 4 alkyl) is optionally replaced by -O(C 1 -C 4 alkyl) substituted;
    R 3为氢； R 3 is hydrogen;
    R 5为氢或者-NHR’； R 5 is hydrogen or -NHR';
    R’选自氢、C 1-C 3烷基和-C(O)C 1-C 3烷基； R' is selected from hydrogen, C 1 -C 3 alkyl and -C(O)C 1 -C 3 alkyl;
    R 4为C 1-C 4卤代烷基； R 4 is C 1 -C 4 haloalkyl;
    R 6为氢或者卤素； R 6 is hydrogen or halogen;
    或者R 4、R 6与它们连接的碳原子一起形成环使S6中的
    Figure PCTCN2022088560-appb-100091
    片段为
    Figure PCTCN2022088560-appb-100092
    Or R 4 , R 6 and the carbon atoms to which they are attached together form a ring so that the
    Figure PCTCN2022088560-appb-100091
    Fragment is
    Figure PCTCN2022088560-appb-100092
    R 7为C 1-C 6烷基； R 7 is C 1 -C 6 alkyl;
    R 8为C 1-C 6烷基。 R 8 is C 1 -C 6 alkyl.
  6. 如权利要求4或5所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、 水合物、溶剂化物、前药和/或其药学上可接受的盐，其中各S结构中的
    Figure PCTCN2022088560-appb-100093
    片段为
    Figure PCTCN2022088560-appb-100094
    Figure PCTCN2022088560-appb-100095
    例如
    Figure PCTCN2022088560-appb-100096
    Figure PCTCN2022088560-appb-100097
    优选为
    Figure PCTCN2022088560-appb-100098
    进一步优选为
    Figure PCTCN2022088560-appb-100099
    The compound of formula I as claimed in claim 4 or 5, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or Its pharmaceutically acceptable salt, wherein each S structure in
    Figure PCTCN2022088560-appb-100093
    Fragment is
    Figure PCTCN2022088560-appb-100094
    Figure PCTCN2022088560-appb-100095
    E.g
    Figure PCTCN2022088560-appb-100096
    Figure PCTCN2022088560-appb-100097
    preferably
    Figure PCTCN2022088560-appb-100098
    more preferably
    Figure PCTCN2022088560-appb-100099
    和/或，R 3为氢； and/or, R 3 is hydrogen;
    和/或，R 7为甲基。 and/or, R7 is methyl.
  7. 如权利要求4所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中所述S6、S6'、S6a或S6c为如下任一结构：The compound of formula I as claimed in claim 4, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceuticals thereof An acceptable salt above, wherein said S6, S6', S6a or S6c is any of the following structures:
    Figure PCTCN2022088560-appb-100100
    Figure PCTCN2022088560-appb-100100
    和/或，所述S6”、S6”'、S6a”或S6c”为如下结构：And/or, the S6", S6"', S6a" or S6c" are the following structures:
    Figure PCTCN2022088560-appb-100101
    Figure PCTCN2022088560-appb-100101
    优选地，所述S为如下结构：Preferably, the S has the following structure:
    Figure PCTCN2022088560-appb-100102
    Figure PCTCN2022088560-appb-100102
    进一步优选地，所述S为如下结构：Further preferably, the S is the following structure:
    Figure PCTCN2022088560-appb-100103
    Figure PCTCN2022088560-appb-100103
  8. 如权利要求1-7中任一项所述式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其特征在于，所述L为-(CH 2) j-，所述-(CH 2) j-中的1个或多个亚甲基任选的被选自-NR 3’-、-O-、-CR 1’R 2’-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NR 3’-、-NR 3’C(O)-、-S(O) 2NR 3’-、-NR 3’S(O) 2-、亚乙烯基、亚乙炔基、苯基、8-10元双环亚芳基、3-7元饱和或部分不饱和的亚环烷基、5-11元的饱和或部分不饱和的亚螺环烷基、5-11元的饱和或部分不饱和的亚稠环烷基、8-10元双环饱和或部分不饱和的亚环烷基、具有1-2个独立地选自氮、氧或硫杂原子的4-7元饱和或部分不饱和的亚杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的5-11元饱和或部分不饱和的亚螺杂环烷基、具有1-2个独立的选自氮、氧或硫杂原子的5-11元饱和或部分不饱和的亚稠杂环烷基、具有1-2个独立地选自氮、氧或硫杂原子的8-10元双环饱和或部分不饱和的亚杂环烷基、具有1-4个独立地选自氮、氧或硫杂原子的5-6元亚杂芳基、或具有1-5个选自氮、氧或硫杂原子的8-10元双环杂芳基的基团替代，所述亚乙烯基、亚乙炔基、亚环烷基、亚杂环烷基、苯基、亚螺杂环烷基、亚稠杂环烷基、亚螺环烷基、亚稠环烷基、亚杂芳基各自独立的任选的被1个或多个选自卤素、氧代、-NR 3’R 4’、-OR 3’、硝基、-CN、C 1-C 6烷基、C 3-C 10环烷基、C 3-C 10杂环烷基的取代基取代，所述烷基、环烷基、杂环烷基任选被1个或多个选自卤素、-OH、-NH 2、-CN、C 1-C 4烷基、C 3-C 6环烷基的取代基取代，R 1’、R 2’各自独立为卤素、-OH、-NH 2、C 1-C 4烷基、C 1-C 4氯代烷基、C 1-C 4羟基烷基、-O(C 1-C 4烷基)、-NH(C 1-C 4烷基)、-NH(C 1-C 4烷基)、C 3-C 6环烷基、-O(C 3-C 6环烷基)、-NH(C 3-C 6环烷基)、C 3-C 6杂环烷基、-O(C 3-C 6杂环烷基)、-NH(C 3-C 6环烷基)；R 3’、R 4’各自独立的为氢、氘、C 1-C 4烷基、C 3-C 6环烷基、C 3-C 6杂环烷基，j为2、3、4、5、6、7、8、9、10、11或12； The compound of formula I according to any one of claims 1-7, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or a pharmaceutically acceptable salt thereof, wherein the L is -(CH 2 ) j -, and one or more methylene groups in the -(CH 2 ) j - are optionally Selected from -NR 3' -, -O-, -CR 1' R 2' -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O- , -OC(O)-, -C(O)NR 3' -, -NR 3' C(O)-, -S(O) 2 NR 3' -, -NR 3' S(O) 2 -, Ethylene, ethynylene, phenyl, 8-10 membered bicyclic arylene, 3-7 membered saturated or partially unsaturated cycloalkylene, 5-11 membered saturated or partially unsaturated spirocycloalkane base, 5-11 membered saturated or partially unsaturated fused cycloalkylene, 8-10 membered bicyclic saturated or partially unsaturated cycloalkylene, with 1-2 members independently selected from nitrogen, oxygen or thia 4-7 membered saturated or partially unsaturated heterocycloalkylene of atoms, 5-11 membered saturated or partially unsaturated spiroheterocycloalkane having 1-2 independent heteroatoms selected from nitrogen, oxygen or sulfur base, 5-11-membered saturated or partially unsaturated fused heterocycloalkylene with 1-2 heteroatoms independently selected from nitrogen, oxygen or sulfur, with 1-2 independently selected from nitrogen, oxygen or sulfur 8-10 membered bicyclic saturated or partially unsaturated heterocycloalkylene with heteroatoms, 5-6 membered heteroarylene with 1-4 heteroatoms independently selected from nitrogen, oxygen or sulfur, or with 1- 5 groups selected from 8-10 membered bicyclic heteroaryl groups of nitrogen, oxygen or sulfur heteroatoms, the vinylidene, ethynylene, cycloalkylene, heterocycloalkylene, phenyl, Spiroheterocycloalkyl, fused heterocycloalkylene, spirocycloalkylene, fused cycloalkylene, and heteroarylene are each independently optionally 1 or more selected from halogen, oxo, -NR Substituent substitution of 3' R 4' , -OR 3' , nitro, -CN, C 1 -C 6 alkyl, C 3 -C 10 cycloalkyl, C 3 -C 10 heterocycloalkyl, said Alkyl, cycloalkyl and heterocycloalkyl are optionally substituted by one or more selected from halogen, -OH, -NH 2 , -CN, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl Substituent substitution, R 1' and R 2' are each independently halogen, -OH, -NH 2 , C 1 -C 4 alkyl, C 1 -C 4 chloroalkyl, C 1 -C 4 hydroxyalkyl, -O(C 1 -C 4 alkyl), -NH(C 1 -C 4 alkyl), -NH(C 1 -C 4 alkyl), C 3 -C 6 cycloalkyl, -O(C 3 -C 6 cycloalkyl), -NH(C 3 -C 6 cycloalkyl), C 3 -C 6 heterocycloalkyl, -O(C 3 -C 6 heterocycloalkyl), -NH(C 3 -C 6 cycloalkyl); R 3' and R 4' are each independently hydrogen, deuterium, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 heterocycloalkyl, and j is 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12;
    优选地，所述L为-(CH 2) j-，所述-(CH 2) j-中的1个、2个、3个4个或者5个亚甲基任选的被选自-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-CHF-、-CHCF 3-、-C(O)-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-、-NCH 3C(O)-、亚乙烯基、亚乙炔基、亚环丙基、亚环丁基、亚环戊基、亚环己基、亚氧杂环丙基、亚氧杂环丁基、亚氧杂环戊基、亚氧杂环己基、亚氮杂环丙基、亚氮杂环丁基、亚氮杂环戊基、亚哌啶基、亚哌嗪基、亚吗啉基、亚高吗啉基、亚苯基、亚吡咯基、亚噻吩基、亚呋喃基、亚咪唑基、亚吡唑基、亚三唑基、亚四唑基、亚噁唑基、亚异噁唑基、亚噻唑基、亚异噻唑基、亚吡啶基、亚嘧啶基、亚哒嗪基、亚吡嗪基、
    Figure PCTCN2022088560-appb-100104
    Figure PCTCN2022088560-appb-100105
    的基团替代，且所述替代基团任选的被1个或多个选自卤素、氧代、-NR 3’R 4’、-OR 3’、C 1-C 4烷基的取代基取代，所述烷基任选被1个或多个选自卤素、-OH、-NH 2的取代基取代，R 3’、R 4’各自独立的为氢、氘、C 1-C 4烷基，j为2、3、4、5、6、7、8、9或者10；     Preferably, the L is -(CH 2 ) j -, and 1, 2, 3, 4 or 5 methylene groups in the -(CH 2 ) j - are optionally selected from -NH -, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -CHF-, -CHCF 3 -, -C(O)-, -C(O)O-, -OC(O)- , -C(O)NH-, -C(O)NCH 3 -, -NHC(O)-, -NCH 3 C(O)-, vinylidene, ethynylene, cyclopropylidene, cyclobutylene , cyclopentylene, cyclohexylene, oxetylene, oxetylene, oxolane, oxetylene, aziridine, azetidine base, azidoline, piperidylene, piperazinylene, morpholinylene, homomorpholinylene, phenylene, pyrrolylene, thienylene, furanylene, imidazolylide, Pyrazolylide, triazolylidene, tetrazolylidene, oxazolylidene, isoxazolylidene, thiazolylidene, isothiazolylidene, pyridylidene, pyrimidinylene, pyridazinylene, pyridine azinyl,
    Figure PCTCN2022088560-appb-100104
    Figure PCTCN2022088560-appb-100105
    and the substitution group is optionally replaced by one or more substituents selected from halogen, oxo, -NR 3' R 4' , -OR 3' , C 1 -C 4 alkyl Substituted, the alkyl group is optionally substituted by one or more substituents selected from halogen, -OH, -NH 2 , R 3' , R 4' are each independently hydrogen, deuterium, C 1 -C 4 alkane base, j is 2, 3, 4, 5, 6, 7, 8, 9 or 10;
    优选地，所述L为-(CH 2) j-，所述-(CH 2) j-中的1个、2个或者3个、4个或者5个亚甲基任选的被选自-NH-、-NCH 3-、-O-、-C(O)-、-C(O)NH-、-NHC(O)-、-NCH 3C(O)-、-C(O)NCH 3-、亚环丙基、亚环丁基、亚环戊基、亚环己基、亚氮杂环丙基、亚氮杂环丁基、亚氮杂环戊基、亚哌啶基、亚哌嗪基、
    Figure PCTCN2022088560-appb-100106
    Figure PCTCN2022088560-appb-100107
    的基团替代，j为5、6、7、8、9或者10。     Preferably, the L is -(CH 2 ) j -, and 1, 2 or 3, 4 or 5 methylene groups in the -(CH 2 ) j - are optionally selected from - NH-, -NCH 3 -, -O-, -C(O)-, -C(O)NH-, -NHC(O)-, -NCH 3 C(O)-, -C(O)NCH 3 -, cyclopropylidene, cyclobutylene, cyclopentylene, cyclohexylene, aziridine, aziridine, aziridine, piperidinylene, piperazine base,
    Figure PCTCN2022088560-appb-100106
    Figure PCTCN2022088560-appb-100107
    group substitution, j is 5, 6, 7, 8, 9 or 10.
  9. 如权利要求8所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述L为The compound of formula I as claimed in claim 8, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceuticals thereof an acceptable salt above, the L is
    Figure PCTCN2022088560-appb-100108
    Figure PCTCN2022088560-appb-100108
    Figure PCTCN2022088560-appb-100109
    Figure PCTCN2022088560-appb-100109
    Figure PCTCN2022088560-appb-100110
    Figure PCTCN2022088560-appb-100110
    Figure PCTCN2022088560-appb-100111
    Figure PCTCN2022088560-appb-100111
    Figure PCTCN2022088560-appb-100112
    Figure PCTCN2022088560-appb-100112
    Figure PCTCN2022088560-appb-100113
    Figure PCTCN2022088560-appb-100113
    Figure PCTCN2022088560-appb-100114
    Figure PCTCN2022088560-appb-100114
    Figure PCTCN2022088560-appb-100115
    Figure PCTCN2022088560-appb-100115
    Figure PCTCN2022088560-appb-100116
    Figure PCTCN2022088560-appb-100116
    Figure PCTCN2022088560-appb-100117
    Figure PCTCN2022088560-appb-100117
    Figure PCTCN2022088560-appb-100118
    Figure PCTCN2022088560-appb-100118
    Figure PCTCN2022088560-appb-100119
    Figure PCTCN2022088560-appb-100119
    Figure PCTCN2022088560-appb-100120
    Figure PCTCN2022088560-appb-100120
    Figure PCTCN2022088560-appb-100121
    Figure PCTCN2022088560-appb-100121
    Figure PCTCN2022088560-appb-100122
    Figure PCTCN2022088560-appb-100122
    Figure PCTCN2022088560-appb-100123
    Figure PCTCN2022088560-appb-100123
    Figure PCTCN2022088560-appb-100124
    Figure PCTCN2022088560-appb-100124
    Figure PCTCN2022088560-appb-100125
    Figure PCTCN2022088560-appb-100125
    Figure PCTCN2022088560-appb-100126
    Figure PCTCN2022088560-appb-100126
    Figure PCTCN2022088560-appb-100127
    Figure PCTCN2022088560-appb-100127
    Figure PCTCN2022088560-appb-100128
    Figure PCTCN2022088560-appb-100128
    Figure PCTCN2022088560-appb-100129
    Figure PCTCN2022088560-appb-100129
    Figure PCTCN2022088560-appb-100130
    Figure PCTCN2022088560-appb-100130
    Figure PCTCN2022088560-appb-100131
    Figure PCTCN2022088560-appb-100131
    Figure PCTCN2022088560-appb-100132
    Figure PCTCN2022088560-appb-100132
  10. 如权利要求1-7中任一项所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述L为LA：The compound of formula I according to any one of claims 1-7, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, pro- A medicine and/or a pharmaceutically acceptable salt thereof, wherein L is LA:
    Figure PCTCN2022088560-appb-100133
    Figure PCTCN2022088560-appb-100133
    其中所述LA中：Where said LA:
    环A为键、C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring A is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
    环B为键、C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或-O-(C 1-C 6烷基)的取代基取代； Ring B is a bond, a C 3 -C 12 cycloalkylene or a 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, the cycloalkylene and heterocycle Alkyl is optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 Substituent substitution of -C 6 alkyl);
    环C为C 3-C 12亚环烷基或含有1-2个选自N、O或S杂原子的3-12元亚杂环烷基，所述亚环烷基和亚杂环烷基任选被选自卤素、氧代、氰基、氨基、羟基、C 1-C 6烷基、C 1-C 6卤代烷基、C 1-C 6羟基烷基或- O-(C 1-C 6烷基)的取代基取代； Ring C is C 3 -C 12 cycloalkylene or 3-12 membered heterocycloalkylene containing 1-2 heteroatoms selected from N, O or S, said cycloalkylene and heterocycloalkylene optionally selected from halogen, oxo, cyano, amino, hydroxy, C1 - C6 alkyl, C1 - C6 haloalkyl, C1 - C6 hydroxyalkyl or -O-( C1 -C 6 alkyl) substituent substitution;
    X”为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-NHC(O)-、-NCH 3C(O)-或-C(O)CH 2O-； X" is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C( O) NCH3- , -NHC(O)-, -NCH3C (O)- or -C(O) CH2O- ;
    L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被选自-O-、-NH-、-C≡C-、-N(C 1-C 6烷基)-、-N(C 1-C 6卤代烷基)-、-C(O)-、-N(C 1-C 6羟基烷基)-或-N(C 3-C 8环烷基)-替代，k为0、1、2、3、4、5、6或7； L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally selected from -O-, -NH-, -C≡C-, -N(C 1 -C 6 alkyl)-, -N(C 1 -C 6 haloalkyl)-, -C(O)-, -N(C 1 -C 6 hydroxyalkyl)- or -N(C 3 -C 8 cycloalkane base)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
    X”'为键、-NH-、-NCH 3-、-O-、-C(CH 3) 2-、-S-、-C＝C-、-C≡C-、-CHF-、-CHCF 3-、-C(O)-、-S(O)-、-S(O) 2-、-C(O)O-、-OC(O)-、-C(O)NH-、-C(O)NCH 3-、-CH 2NCH 3-、-NHC(O)-或-NCH 3C(O)-。 X"' is a bond, -NH-, -NCH 3 -, -O-, -C(CH 3 ) 2 -, -S-, -C=C-, -C≡C-, -CHF-, -CHCF 3 -, -C(O)-, -S(O)-, -S(O) 2 -, -C(O)O-, -OC(O)-, -C(O)NH-, -C (O) NCH3- , -CH2NCH3- , -NHC(O) - or -NCH3C (O)-.
  11. 如权利要求10所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述LA中环A为3-6元饱和的亚环烷基；环B含有1个或者2个氮杂原子的4-7元饱和的单环亚杂环烷基；环C为含有1个或者2个氮杂原子的4-7元饱和的单环亚杂环烷基、含有1个或者2个氮杂原子的7-11元的亚螺杂环烷基或者亚稠杂环烷基；X”为键或-C(O)-；L 3为-(CH 2) k，k为1、2、3、4或者5。 The compound of formula I as claimed in claim 10, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceuticals The acceptable salt above, in the LA, ring A is a 3-6 membered saturated cycloalkylene; ring B contains a 4-7 membered saturated monocyclic heterocycloalkylene with 1 or 2 nitrogen heteroatoms; ring C is a 4-7 membered saturated monocyclic heterocycloalkylene containing 1 or 2 nitrogen heteroatoms, a 7-11 membered spiroheterocycloalkylene containing 1 or 2 nitrogen heteroatoms, or a fused Heterocycloalkyl; X" is a bond or -C(O)-; L 3 is -(CH 2 ) k , and k is 1, 2, 3, 4 or 5.
  12. 如权利要求10所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述LA为LA-1：The compound of formula I as claimed in claim 10, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceutics On an acceptable salt, the LA is LA-1:
    Figure PCTCN2022088560-appb-100134
    Figure PCTCN2022088560-appb-100134
    其中，所述LA-1中，环A、环B、环C、L 3、X”如权利要求10中所定义和描述。 Wherein, in the LA-1, ring A, ring B, ring C, L 3 , X" are as defined and described in claim 10 .
  13. 如权利要求10所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中，所述LA为LA-2、LA-3、LA-4或LA-5：The compound of formula I as claimed in claim 10, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceutics An acceptable salt of the above, wherein the LA is LA-2, LA-3, LA-4 or LA-5:
    Figure PCTCN2022088560-appb-100135
    Figure PCTCN2022088560-appb-100135
    其中所述LA-2中，环A为
    Figure PCTCN2022088560-appb-100136
    Figure PCTCN2022088560-appb-100137
    其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代；     wherein in the LA-2, ring A is
    Figure PCTCN2022088560-appb-100136
    Figure PCTCN2022088560-appb-100137
    wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
    X”'为-C(O)-；X"' is -C(O)-;
    环B为
    Figure PCTCN2022088560-appb-100138
    其中c端与X”'连接，d端与L 3连接；所述环B中的1、2、3或4个氢原子任选被F取代；     Ring B is
    Figure PCTCN2022088560-appb-100138
    wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
    L 3为-(CH 2) k-，其中所述L 3中包含的一个或两个CH 2各自独立地任选的被-O-、-NH-或-N(C 1-C 6烷基)-替代，或者所述L 3中包含的一个-CH 2CH 2-任选的被-C≡C-替代；k为1、2、3或4； L 3 is -(CH 2 ) k -, wherein one or two CH 2 contained in said L 3 are each independently optionally -O-, -NH- or -N(C 1 -C 6 alkyl )-replace, or one -CH 2 CH 2 - included in the L 3 is optionally replaced by -C≡C-; k is 1, 2, 3 or 4;
    环C为
    Figure PCTCN2022088560-appb-100139
    其中e端与 L 3连接，f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代；     Ring C is
    Figure PCTCN2022088560-appb-100139
    Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
    X”为-C(O)-；X" is -C(O)-;
    Figure PCTCN2022088560-appb-100140
    Figure PCTCN2022088560-appb-100140
    其中，所述LA-3中，环A为
    Figure PCTCN2022088560-appb-100141
    Figure PCTCN2022088560-appb-100142
    其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代；     Wherein, in the LA-3, ring A is
    Figure PCTCN2022088560-appb-100141
    Figure PCTCN2022088560-appb-100142
    wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
    X”'为-C(O)-；X"' is -C(O)-;
    环B为
    Figure PCTCN2022088560-appb-100143
    其中c端与X”'连接，d端与L 3连接；所述环B中的1、2、3或4个氢原子任选被F取代；     Ring B is
    Figure PCTCN2022088560-appb-100143
    wherein the c-terminal is connected with X"', and the d-terminal is connected with L; 1, 2, 3 or 4 hydrogen atoms in the ring B are optionally substituted by F;
    L 3为-(CH 2) k-，其中所述L 3中包含的一个CH 2任选的被-O-、-NH-或-N(C 1-C 6烷基)-替代；k为1或2； L 3 is -(CH 2 ) k -, wherein one CH 2 contained in said L 3 is optionally replaced by -O-, -NH- or -N(C 1 -C 6 alkyl)-; k is 1 or 2;
    环C为
    Figure PCTCN2022088560-appb-100144
    其中e端与L 3连接，f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代；     Ring C is
    Figure PCTCN2022088560-appb-100144
    Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
    X”为-C(O)-；X" is -C(O)-;
    Figure PCTCN2022088560-appb-100145
    Figure PCTCN2022088560-appb-100145
    其中，所述LA-4中，Wherein, in the LA-4,
    环A为
    Figure PCTCN2022088560-appb-100146
    Figure PCTCN2022088560-appb-100147
    其中a端与S连接，b端与X”'连接；所述环A中的1、2、3或4个氢原子任选被F取代；     Ring A is
    Figure PCTCN2022088560-appb-100146
    Figure PCTCN2022088560-appb-100147
    wherein the a-end is connected to S, and the b-end is connected to X"'; 1, 2, 3 or 4 hydrogen atoms in the ring A are optionally substituted by F;
    X”'为键、-C(O)NH-或-C(O)NCH 3-； X"' is a bond, -C(O)NH- or -C(O)NCH 3 -;
    环B为键；Ring B is a bond;
    L 3为-(CH 2) k，所述L 3中的一个或两个亚甲基任选的被-O-、-NH-、-C(O)-、-C≡C-或-N(C 1-C 6烷基)-替 代，k为0、1、2、3、4、5、6或7； L 3 is -(CH 2 ) k , and one or two methylene groups in said L 3 are optionally -O-, -NH-, -C(O)-, -C≡C- or -N (C 1 -C 6 alkyl)-substitution, k is 0, 1, 2, 3, 4, 5, 6 or 7;
    环C为
    Figure PCTCN2022088560-appb-100148
    Figure PCTCN2022088560-appb-100149
    其中e端与L 3连接，f端与X”连接；所述环C中的1、2、3或4个氢原子任选被F取代；     Ring C is
    Figure PCTCN2022088560-appb-100148
    Figure PCTCN2022088560-appb-100149
    Wherein the e end is connected with L , and the f end is connected with X "; 1, 2, 3 or 4 hydrogen atoms in the ring C are optionally substituted by F;
    X”为-C(O)-；X" is -C(O)-;
    Figure PCTCN2022088560-appb-100150
    Figure PCTCN2022088560-appb-100150
    其中，环A、X”'、环B、L 3和环C如LA-2或LA-3中所定义； wherein Ring A, X"', Ring B, L and Ring C are as defined in LA-2 or LA-3;
    X”为-C(O)CH 2O-，X”中的-C(O)-与环C连接。 X" is -C(O)CH 2 O-, and -C(O)- in X" is connected to ring C.
  14. 如权利要求13所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中，所述LA-2中，环A为
    Figure PCTCN2022088560-appb-100151
    Figure PCTCN2022088560-appb-100152
    其中a端与S连接，b端与X”'连接；     The compound of formula I as claimed in claim 13, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceutics The acceptable salt above, wherein, in the LA-2, ring A is
    Figure PCTCN2022088560-appb-100151
    Figure PCTCN2022088560-appb-100152
    The a-end is connected to S, and the b-end is connected to X"';
    和/或，所述LA-2中，环B为
    Figure PCTCN2022088560-appb-100153
    其中c端与X”'连接，d端与L 3连接；     And/or, in described LA-2, ring B is
    Figure PCTCN2022088560-appb-100153
    Wherein the c end is connected with X "', and the d end is connected with L 3 ;
    和/或，所述LA-2中，L 3为-CH 2-、-(CH 2) 2-、-(CH 2) 3-、-(CH 2) 4-、
    Figure PCTCN2022088560-appb-100154
    Figure PCTCN2022088560-appb-100155
    其中k”端与环B连接，k'端与环C连接；     And/or, in the LA-2, L 3 is -CH 2 -, -(CH 2 ) 2 -, -(CH 2 ) 3 -, -(CH 2 ) 4 -,
    Figure PCTCN2022088560-appb-100154
    Figure PCTCN2022088560-appb-100155
    Wherein the k" end is connected to the ring B, and the k' end is connected to the ring C;
    和/或，所述LA-2中，环C为
    Figure PCTCN2022088560-appb-100156
    其中e端与L 3连接，f端与X”连接；     And/or, in described LA-2, ring C is
    Figure PCTCN2022088560-appb-100156
    Wherein the e end is connected with L3, and the f end is connected with X";
    和/或，所述LA-3中，环A为
    Figure PCTCN2022088560-appb-100157
    其中a端与S连接，b端与X”'连接；     And/or, in described LA-3, ring A is
    Figure PCTCN2022088560-appb-100157
    The a-end is connected to S, and the b-end is connected to X"';
    和/或，所述LA-3中，环B为
    Figure PCTCN2022088560-appb-100158
    其中c端与X”'连接，d端与L 3连接；     And/or, in described LA-3, ring B is
    Figure PCTCN2022088560-appb-100158
    Wherein the c end is connected with X "', and the d end is connected with L 3 ;
    和/或，所述LA-3中，L 3为-(CH 2) k-，k为1或2； And/or, in the LA-3, L 3 is -(CH 2 ) k -, and k is 1 or 2;
    和/或，所述LA-3中，环C为
    Figure PCTCN2022088560-appb-100159
    其中e端与L 3连接，f端与X”连接；     And/or, in described LA-3, ring C is
    Figure PCTCN2022088560-appb-100159
    Wherein the e end is connected with L3, and the f end is connected with X";
    和/或，所述LA-4中，环A为
    Figure PCTCN2022088560-appb-100160
    其中a端与S连接，b端与X”'连接；     And/or, in described LA-4, ring A is
    Figure PCTCN2022088560-appb-100160
    The a-end is connected to S, and the b-end is connected to X"';
    和/或，所述LA-4中，L 3为-CH 2-、-(CH 2) 2-、
    Figure PCTCN2022088560-appb-100161
    Figure PCTCN2022088560-appb-100162
    其中k”端与环B连接，k'端与环C连接；     And/or, in the LA-4, L 3 is -CH 2 -, -(CH 2 ) 2 -,
    Figure PCTCN2022088560-appb-100161
    Figure PCTCN2022088560-appb-100162
    Wherein the k" end is connected to the ring B, and the k' end is connected to the ring C;
    和/或，所述LA-4中，环C为
    Figure PCTCN2022088560-appb-100163
    其中e端与L 3连接，f端与X”连接；     And/or, in described LA-4, ring C is
    Figure PCTCN2022088560-appb-100163
    Wherein the e end is connected with L3, and the f end is connected with X";
    和/或，所述LA-5中，环A为
    Figure PCTCN2022088560-appb-100164
    其中a端与S连接，b端与X”'连接；     And/or, in described LA-5, ring A is
    Figure PCTCN2022088560-appb-100164
    The a-end is connected to S, and the b-end is connected to X"';
    和/或，所述LA-5中，环B为
    Figure PCTCN2022088560-appb-100165
    其中c端与X”'连接，d端与L 3连接；     And/or, in described LA-5, ring B is
    Figure PCTCN2022088560-appb-100165
    Wherein the c end is connected with X"', and the d end is connected with L 3 ;
    和/或，所述LA-5中，L 3为-(CH 2)-； And/or, in the LA-5, L 3 is -(CH 2 )-;
    和/或，所述LA-5中，环C为
    Figure PCTCN2022088560-appb-100166
    其中e端与L 3连接，f端与X”连接。     And/or, in described LA-5, ring C is
    Figure PCTCN2022088560-appb-100166
    The e end is connected to L 3 and the f end is connected to X".
  15. 如权利要求10或13所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述LA为如下任一结构：The compound of formula I as claimed in claim 10 or 13, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or Its pharmaceutically acceptable salt, the LA is any of the following structures:
    Figure PCTCN2022088560-appb-100167
    Figure PCTCN2022088560-appb-100167
    Figure PCTCN2022088560-appb-100168
    Figure PCTCN2022088560-appb-100168
    Figure PCTCN2022088560-appb-100169
    Figure PCTCN2022088560-appb-100169
    优选地，所述LA为如下任一结构：Preferably, the LA is any of the following structures:
    Figure PCTCN2022088560-appb-100170
    Figure PCTCN2022088560-appb-100170
    Figure PCTCN2022088560-appb-100171
    Figure PCTCN2022088560-appb-100171
  16. 如权利要求1-15中任一项所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述E为E21：The compound of formula I according to any one of claims 1-15, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, pro- Medicine and/or its pharmaceutically acceptable salt, said E is E21:
    Figure PCTCN2022088560-appb-100172
    Figure PCTCN2022088560-appb-100172
    其中所述E21中：Among the E21:
    X”为C或N；X" is C or N;
    Y”为C、N、O或者S；Y" is C, N, O or S;
    Q 1、Q 2、Q 3、Q 4、Q 5各自独立的为CR 3”或N； Q 1 , Q 2 , Q 3 , Q 4 , Q 5 are independently CR 3 ″ or N;
    R 3”各自独立的为氢、氘、羟基、氨基、氰基、卤素、C 1-C 6烷基、C 3-C 8环烷基、3-8元杂环烷基、6-10元芳基、5-10元杂芳基、-O(C 1-C 6烷基)、-O-(C 3-C 8环烷基)、-O-(3-8元杂环烷基)、N(C 1-C 6烷基) 1-2、NH(C 3-C 8环烷基)、NH(3-8元杂环烷基)、-O-(6-10芳基)、-O-(5-10元杂芳基)；所述烷基、环烷基、杂环烷基、芳基、杂芳基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代； R 3 " is each independently hydrogen, deuterium, hydroxyl, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, 6-10 membered Aryl, 5-10 membered heteroaryl, -O(C 1 -C 6 alkyl), -O-(C 3 -C 8 cycloalkyl), -O-(3-8 membered heterocycloalkyl) , N(C 1 -C 6 alkyl) 1-2 , NH(C 3 -C 8 cycloalkyl), NH(3-8 membered heterocycloalkyl), -O-(6-10 aryl), -O-(5-10 membered heteroaryl); the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally selected by 1-3 independently selected from hydroxyl, halogen, cyano group, amino group substitution;
    m”为1、2或3；m" is 1, 2 or 3;
    R 1”各自独立的为氢、氘、羟基、氨基、氰基、卤素、C 1-C 6烷基、C 3-C 8环烷基、3-8元杂环烷基、6-10元芳基、5-10元杂芳基、-O(C 1-C 6烷基)，所述烷基、环烷基、杂环烷基、芳基、杂芳基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代； R 1 " is independently hydrogen, deuterium, hydroxyl, amino, cyano, halogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 3-8 membered heterocycloalkyl, 6-10 membered Aryl, 5-10 membered heteroaryl, -O(C 1 -C 6 alkyl), the alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl are optionally substituted by 1-3 substituted with groups independently selected from hydroxyl, halogen, cyano, amino;
    R 2”为氢、氘、C 1-C 6烷基或者C 3-C 6环烷基，所述C 1-C 6烷基和C 3-C 6环烷基任选的被1-3个独立的选自羟基、卤素、氰基、氨基的基团取代。 R 2 " is hydrogen, deuterium, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, and the C 1 -C 6 alkyl and C 3 -C 6 cycloalkyl are optionally surrounded by 1-3 substituted with a group independently selected from hydroxy, halogen, cyano, amino.
  17. 如权利要求16所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述E21具有式E21-1a、E21-1b、E21-1c、E21-1d、E21-1e、E21-1f、E21-1g、E21-1aa、E21-1bb、E21-1cc、E21-1dd、E21-1ee、E21-1ff或E21-1gg结构：The compound of formula I as claimed in claim 16, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceuticals thereof Acceptable salts above, the E21 has formula E21-1a, E21-1b, E21-1c, E21-1d, E21-1e, E21-1f, E21-1g, E21-1aa, E21-1bb, E21-1cc , E21-1dd, E21-1ee, E21-1ff or E21-1gg structure:
    Figure PCTCN2022088560-appb-100173
    Figure PCTCN2022088560-appb-100173
    Figure PCTCN2022088560-appb-100174
    Figure PCTCN2022088560-appb-100174
    其中所述Q 1、Q 2、Q 3、Q 4、Q 5、R 1”、R 2”、R 3”、m”如权利要求16中所定义和描述。 wherein said Q1, Q2 , Q3 , Q4 , Q5 , R1", R2 ", R3 ", m " are as defined and described in claim 16 .
  18. 如权利要求17所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中所述E21具有式E21-1h、E21-1i、E21-1j或E21-1hh结构，优选为E21-1h：The compound of formula I according to claim 17, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceutics An acceptable salt of the above, wherein the E21 has the structure of formula E21-1h, E21-1i, E21-1j or E21-1hh, preferably E21-1h:
    Figure PCTCN2022088560-appb-100175
    Figure PCTCN2022088560-appb-100175
    其中，R 3”如权利要求17中所定义。 wherein R 3 " is as defined in claim 17 .
  19. 如权利要求16-18中任一项所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中，R 3”为氢、卤素、C 1-C 6烷基或-O(C 1-C 6烷基)，所述C 1-C 6烷基和-O(C 1-C 6烷基)任选被1-3个卤素取代，例如氢、F、Cl、CF 3、-OCF 3或-OCH 3。 The compound of formula I according to any one of claims 16-18, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, pro- Medicine and/or a pharmaceutically acceptable salt thereof, wherein R 3 " is hydrogen, halogen, C 1 -C 6 alkyl or -O(C 1 -C 6 alkyl), the C 1 -C 6 alkyl and -O( C1 - C6 alkyl) are optionally substituted with 1-3 halogens, such as hydrogen, F, Cl, CF3 , -OCF3 or -OCH3 .
  20. 如权利要求16所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述E21为：The compound of formula I as claimed in claim 16, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceutics On acceptable salts, the E21 is:
    Figure PCTCN2022088560-appb-100176
    Figure PCTCN2022088560-appb-100176
    优选地，所述E21为如下任一结构：Preferably, the E21 is any of the following structures:
    Figure PCTCN2022088560-appb-100177
    Figure PCTCN2022088560-appb-100177
    Figure PCTCN2022088560-appb-100178
    Figure PCTCN2022088560-appb-100178
  21. 如权利要求1所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，所述式Ⅰ化合物为如下任一化合物：The compound of formula I as claimed in claim 1, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or its pharmaceuticals An acceptable salt of the above, the compound of formula I is any of the following compounds:
    Figure PCTCN2022088560-appb-100179
    Figure PCTCN2022088560-appb-100179
    Figure PCTCN2022088560-appb-100180
    Figure PCTCN2022088560-appb-100180
    Figure PCTCN2022088560-appb-100181
    Figure PCTCN2022088560-appb-100181
    Figure PCTCN2022088560-appb-100182
    Figure PCTCN2022088560-appb-100182
    Figure PCTCN2022088560-appb-100183
    Figure PCTCN2022088560-appb-100183
    Figure PCTCN2022088560-appb-100184
    Figure PCTCN2022088560-appb-100184
    Figure PCTCN2022088560-appb-100185
    Figure PCTCN2022088560-appb-100185
    Figure PCTCN2022088560-appb-100186
    Figure PCTCN2022088560-appb-100186
    Figure PCTCN2022088560-appb-100187
    Figure PCTCN2022088560-appb-100187
    Figure PCTCN2022088560-appb-100188
    Figure PCTCN2022088560-appb-100188
  22. 如权利要求1所述的式Ⅰ化合物、和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，其中所述氘代化物具有如下任一结构：The compound of formula I as claimed in claim 1, and/or its stereoisomers, enantiomers, diastereomers, deuterated compounds, hydrates, solvates, prodrugs and/or pharmaceuticals thereof An acceptable salt above, wherein the deuterated compound has any of the following structures:
    Figure PCTCN2022088560-appb-100189
    Figure PCTCN2022088560-appb-100189
  23. 一种药物组合物，其包含权利要求1-22任一项所述化合物，和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐，以及药学上可接受的载体、稀释剂或赋形剂。A pharmaceutical composition comprising the compound described in any one of claims 1-22, and/or its stereoisomer, enantiomer, diastereomer, deuterated compound, hydrate, solvent compounds, prodrugs and/or pharmaceutically acceptable salts thereof, and pharmaceutically acceptable carriers, diluents or excipients.
  24. 一种权利要求1-22任一项所述化合物，和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐或权利要求23所述的药物组合物在制备用于治疗和/或预防SOS1介导的疾病或病症、或由SOS1与Ras或者SOS1与Rac相互作用所引起的疾病或病症、或癌症的药物中的应用。A compound described in any one of claims 1-22, and/or a stereoisomer, enantiomer, diastereomer, deuterated compound, hydrate, solvate, prodrug and/or thereof Or a pharmaceutically acceptable salt thereof or the pharmaceutical composition of claim 23 in preparation for the treatment and/or prevention of a disease or condition mediated by SOS1, or a disease caused by the interaction of SOS1 and Ras or SOS1 and Rac or disease, or the application in the medicine of cancer.
  25. 如权利要求24中所述的应用，其中所述癌症选自：The use as claimed in claim 24, wherein the cancer is selected from:
    心脏:肉瘤(血管肉瘤、纤维肉瘤、横纹肌肉瘤、脂肪肉瘤)、黏液瘤、横纹肌瘤、纤维瘤、脂肪瘤和畸胎瘤组；Cardiac: Sarcomas (angiosarcoma, fibrosarcoma, rhabdomyosarcoma, liposarcoma), myxoma, rhabdomyomas, fibroids, lipomas and teratoma groups;
    肺:支气管癌(鳞状细胞癌、未分化小细胞癌、未分化大细胞癌、腺癌)、肺泡癌(细支气管癌)、支气管腺瘤、肉瘤、淋巴瘤、软骨瘤错构瘤、间皮瘤；Lung: Bronchial carcinoma (squamous cell carcinoma, undifferentiated small cell carcinoma, undifferentiated large cell carcinoma, adenocarcinoma), alveolar carcinoma (bronchiolar carcinoma), bronchial adenoma, sarcoma, lymphoma, chondroma, hamartoma, interstitial carcinoma skin tumor;
    胃肠道食管(鳞状细胞癌、腺癌、平滑肌肉瘤、淋巴瘤)、胃(癌、淋巴瘤、平滑肌肉瘤)、胰腺(导管腺癌、胰岛素瘤、胰高血糖素瘤、胃泌素瘤、类癌肿瘤、血管活性肠肽瘤)、小肠(腺癌、淋巴瘤、类癌肿瘤、卡波西氏肉瘤、平滑肌瘤、血管瘤、脂肪瘤、神经纤维瘤、纤维瘤)、大肠(腺癌、管状腺瘤、绒毛腺瘤、错构瘤、平滑肌瘤)；Gastrointestinal esophagus (squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma), stomach (cancer, lymphoma, leiomyosarcoma), pancreas (ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma , carcinoid tumor, vasoactive intestinal peptide tumor), small intestine (adenocarcinoma, lymphoma, carcinoid tumor, Kaposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, fibroma), large intestine ( adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, leiomyoma);
    泌尿生殖系统:肾(腺癌、肾母细胞瘤、淋巴瘤、白血病)、膀胱和尿道(鳞状细胞癌、移行细胞癌、腺癌)、前列腺(腺癌、肉瘤)、睾丸(精原细胞瘤、畸胎瘤、胚胎癌、畸胎瘤、绒毛膜癌、肉瘤、间质细胞癌、纤维瘤、纤维腺瘤、腺瘤样瘤、脂肪瘤)；Genitourinary System: Kidney (adenocarcinoma, Wilms tumor, lymphoma, leukemia), bladder and urethra (squamous cell carcinoma, transitional cell carcinoma, adenocarcinoma), prostate (adenocarcinoma, sarcoma), testis (spermatogonia) tumor, teratoma, embryonal carcinoma, teratoma, choriocarcinoma, sarcoma, mesenchymal cell carcinoma, fibroma, fibroadenoma, adenomatous tumor, lipoma);
    肝:肝癌(肝细胞癌)、胆管癌、肝母细胞瘤、血管肉瘤、肝细胞腺瘤、血管瘤；Liver: liver cancer (hepatocellular carcinoma), cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, hemangioma;
    胆道:胆囊癌、壶腹癌、胆管癌；Biliary tract: gallbladder cancer, ampullary cancer, cholangiocarcinoma;
    骨:骨肉瘤(骨肉瘤)、纤维肉瘤、恶性纤维组织细胞瘤、软骨肉瘤、尤因氏肉瘤、恶性淋巴瘤(网状细胞肉瘤)、多发性骨髓瘤、恶性巨细胞瘤脊索瘤、软骨瘤(骨软骨外生骨病)、良性软骨瘤、成软骨瘤、软骨黏液纤维瘤、骨样骨瘤和巨细胞瘤；Bone: Osteosarcoma (osteosarcoma), fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma, malignant giant cell tumor chordoma, chondroma (extrachondral bone disease), benign chondroma, chondroblastoma, chondromyxofibroma, osteoid osteoma, and giant cell tumor;
    神经系统:颅骨(骨瘤、血管瘤、肉芽肿、黄色瘤、畸形骨炎)、脑膜(脑膜瘤、脑膜肉瘤、胶质瘤)、大脑(星形细胞瘤、髓母细胞瘤、胶质瘤、室管膜瘤、生发细胞瘤(松果体瘤)、多形胶质母细胞瘤、少突胶质母细胞瘤、神经鞘瘤、视网膜母细胞瘤、先天性肿瘤)、脊髓神经纤维瘤、脑膜瘤、胶质瘤、肉瘤)；Nervous system: skull (osteomas, hemangiomas, granulomas, xanthomas, osteitis malformations), meninges (meningiomas, meningiosarcomas, gliomas), brain (astrocytomas, medulloblastomas, gliomas) , ependymoma, germinoma (pineal tumor), glioblastoma multiforme, oligodendroglioma, schwannoma, retinoblastoma, congenital tumors), spinal neurofibromas , meningioma, glioma, sarcoma);
    妇科:子宫(子宫内膜癌(浆液性囊腺癌、粘液性囊腺癌、未分类癌)、颗粒-鞘膜细胞瘤、支持间质细胞瘤、无生殖细胞瘤、恶性畸胎瘤)、外阴(鳞状细胞癌、上皮内癌、腺癌、纤维肉瘤、黑素瘤)、阴道(透明细胞癌、鳞状细胞癌、葡萄状肉瘤(胚胎型横纹肌肉瘤)、输卵管(癌)；Gynecology: Uterine (endometrial carcinoma (serous cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified carcinoma), granular-schingmocytoma, Sertoli stromal cell tumor, germ cell tumor, malignant teratoma), Vulva (squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, melanoma), vagina (clear cell carcinoma, squamous cell carcinoma, grape sarcoma (embryonic rhabdomyosarcoma), fallopian tube (cancer);
    血液学:血液(髓系白血病(急性和慢性)、急性淋巴母细胞白血病、慢性淋巴细胞白血病、骨髓增生性疾病、多发性骨髓瘤、骨髓增生异常综合征)、霍奇金病、非霍奇金淋巴瘤(恶性淋巴瘤)；Hematology: Hematology (myeloid leukemia (acute and chronic), acute lymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferative disorders, multiple myeloma, myelodysplastic syndromes), Hodgkin's disease, non-Hodgkin's Golden lymphoma (malignant lymphoma);
    皮肤:恶性黑色素瘤、基底细胞癌、鳞状细胞癌、卡波西肉瘤、痣发育不良痣、脂肪瘤、血管瘤、皮肤纤维瘤、瘢痕疙瘩、银屑病；Skin: malignant melanoma, basal cell carcinoma, squamous cell carcinoma, Kaposi's sarcoma, nevus dysplasia, lipoma, hemangioma, dermatofibroma, keloid, psoriasis;
    肾上腺:成神经细胞瘤。Adrenal gland: neuroblastoma.
  26. 如权利要求24中所述的应用，其中，所述癌症为胰腺癌、肺癌、结肠直肠癌、胆管上皮癌、多发性骨髓瘤、黑色素瘤、子宫癌、子宫内膜癌、甲状腺癌、急性髓性白血病、膀胱癌、尿路上皮癌、胃癌、子宫颈癌、头颈部鳞状细胞癌、弥漫性大B细胞淋巴瘤、食道癌、慢性淋巴细胞性白血病、肝细胞癌、乳腺癌、卵巢癌、前列腺癌、成胶质细胞瘤、肾癌或肉瘤。The use as claimed in claim 24, wherein the cancer is pancreatic cancer, lung cancer, colorectal cancer, bile duct epithelial cancer, multiple myeloma, melanoma, uterine cancer, endometrial cancer, thyroid cancer, acute myeloid cancer leukemia, bladder cancer, urothelial cancer, gastric cancer, cervical cancer, head and neck squamous cell carcinoma, diffuse large B-cell lymphoma, esophageal cancer, chronic lymphocytic leukemia, hepatocellular carcinoma, breast cancer, ovary cancer, prostate cancer, glioblastoma, kidney cancer or sarcoma.
  27. 一种权利要求1-22任一项所述化合物，和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐或权利要求23所述的药物组合物在制备治疗和/预防1型神经纤维瘤病(NF1)、努南综合征(NS)、伴有多雀斑的努南综合征(NSML)、毛细血管畸形-动静脉畸形综合征(CM-AVM)、科斯特洛综合征(CS)、心-面-皮肤综合症(CFC)、莱格斯综合征和遗传性牙龈纤维瘤病药物的应用。A compound described in any one of claims 1-22, and/or a stereoisomer, enantiomer, diastereomer, deuterated compound, hydrate, solvate, prodrug and/or thereof Or a pharmaceutically acceptable salt thereof or the pharmaceutical composition of claim 23 in the preparation of treatment and/prevention of neurofibromatosis type 1 (NF1), Noonan syndrome (NS), Noonan syndrome with multiple freckles Syndrome (NSML), Capillary Malformation-Arteriovenous Malformation Syndrome (CM-AVM), Costello Syndrome (CS), Cardiofacial-cutaneous Syndrome (CFC), Leggers Syndrome and Hereditary Gingival Fibrosis The application of oncology drugs.
  28. 一种权利要求1-22任一项所述化合物，和/或其立体异构体、对映异构体、非对映异构体、氘代化物、水合物、溶剂化物、前药和/或其药学上可接受的盐或权利要求23所述的药物组合物在制备用于治疗 和/或预防KRAS介导的疾病或病症的药物中的应用，所述的KRAS优选为突变型KRAS，所述突变型KRAS优选为KRAS G12C、KRAS G12D、KRAS G13D和KRAS G12V中的一种或多种。A compound described in any one of claims 1-22, and/or a stereoisomer, enantiomer, diastereomer, deuterated compound, hydrate, solvate, prodrug and/or thereof or the application of a pharmaceutically acceptable salt thereof or the pharmaceutical composition according to claim 23 in the preparation of a medicine for the treatment and/or prevention of a disease or condition mediated by KRAS, wherein the KRAS is preferably a mutant KRAS, The mutant KRAS is preferably one or more of KRAS G12C, KRAS G12D, KRAS G13D and KRAS G12V.
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